UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-Q
(Mark One)
☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the Quarterly Period Ended March 31, 2026
or
☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from ______ to ______
Commission file number: 001-37717
Senseonics Holdings, Inc.
(Exact name of registrant as specified in its charter)
Delaware |
3841 |
47-1210911 |
20451 Seneca Meadows Parkway
Germantown, MD 20876-7005
(301) 515-7260
(Address, including zip code, and telephone number, including area code, of registrant’s principal executive offices)
Securities registered pursuant to Section 12(b) of the Securities Exchange Act of 1934:
Common Stock, $0.001 par value |
SENS |
Nasdaq Stock Market LLC |
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No ☒
There were 41,802,965 shares of common stock, par value $0.001, outstanding as of May 4, 2026.
TABLE OF CONTENTS
PART I: Financial Information |
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ITEM 1: Financial Statements |
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Condensed Consolidated Balance Sheets as of March 31, 2026 (Unaudited) and December 31, 2025 |
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3 |
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4 |
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5 |
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6 |
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Notes to Unaudited Condensed Consolidated Financial Statements |
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7 |
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ITEM 2: Management’s Discussion and Analysis of Financial Condition and Results of Operations |
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27 |
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ITEM 3: Quantitative and Qualitative Disclosures About Market Risk |
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37 |
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37 |
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38 |
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38 |
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38 |
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ITEM 2: Unregistered Sales of Equity Securities and Use of Proceeds |
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40 |
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40 |
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40 |
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40 |
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41 |
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43 |
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2
Senseonics Holdings, Inc.
Condensed Consolidated Balance Sheets
(in thousands, except share and per share data)
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March 31, |
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December 31, |
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2026 |
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2025 |
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(unaudited) |
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Assets |
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Current assets: |
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Cash and cash equivalents |
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$ |
29,612 |
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$ |
40,234 |
Restricted cash |
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315 |
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315 |
Short term investments, net |
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34,709 |
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53,796 |
Accounts receivable, net |
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10,655 |
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6,807 |
Accounts receivable, net - related parties |
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4,056 |
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5,312 |
Inventory, net |
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8,308 |
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6,703 |
Prepaid expenses and other current assets |
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4,626 |
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4,366 |
Total current assets |
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92,281 |
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117,533 |
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Deposits and other assets |
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6,429 |
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4,536 |
Property, equipment and intangible assets, net |
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4,147 |
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4,200 |
Total assets |
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$ |
102,857 |
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$ |
126,269 |
Liabilities and Stockholders’ Equity |
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Current liabilities: |
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Accounts payable |
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$ |
3,188 |
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$ |
4,059 |
Accrued expenses and other current liabilities |
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15,097 |
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15,091 |
Accrued expenses and other current liabilities, related parties |
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8,040 |
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5,198 |
Total current liabilities |
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26,325 |
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24,348 |
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Long-term debt and notes payables, net |
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35,912 |
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35,586 |
Non-current operating lease liabilities |
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6,285 |
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5,289 |
Total liabilities |
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68,522 |
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65,223 |
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Commitments and contingencies |
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Stockholders’ equity: |
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Common stock, $0.001 par value per share; 70,000,000 shares authorized as of March 31, 2026 and December 31, 2025; 41,795,466 shares and 41,265,778 shares issued and outstanding as of March 31, 2026 and December 31, 2025 |
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42 |
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41 |
Additional paid-in capital |
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1,083,605 |
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1,077,923 |
Accumulated other comprehensive income |
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8 |
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69 |
Accumulated deficit |
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(1,049,320) |
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(1,016,987) |
Total stockholders’ equity |
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34,335 |
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61,046 |
Total liabilities and stockholders’ equity |
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$ |
102,857 |
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$ |
126,269 |
The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.
3
Senseonics Holdings, Inc.
Unaudited Condensed Consolidated Statements of Operations and Comprehensive Loss
(in thousands, except share and per share data)
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Three Months Ended |
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March 31, |
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2026 |
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2025 |
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Revenue, net |
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$ |
9,341 |
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$ |
1,810 |
Revenue, net - related parties |
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2,370 |
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4,447 |
Total revenue |
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11,711 |
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6,257 |
Cost of sales |
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4,771 |
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4,752 |
Gross profit |
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6,940 |
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1,505 |
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Expenses: |
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Research and development expenses |
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8,611 |
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7,299 |
Selling, general and administrative expenses |
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30,175 |
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7,694 |
Operating loss |
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(31,846) |
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(13,488) |
Other income (expense), net: |
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Interest income |
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742 |
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675 |
Interest expense |
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(1,192) |
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(1,429) |
Other expense |
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(37) |
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(17) |
Total other income (expense), net |
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(487) |
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(771) |
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Net Loss |
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(32,333) |
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(14,259) |
Other comprehensive loss |
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Unrealized loss on marketable securities |
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(61) |
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(3) |
Other comprehensive loss |
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(61) |
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(3) |
Total comprehensive loss |
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$ |
(32,394) |
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$ |
(14,262) |
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Basic net loss per common share |
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$ |
(0.71) |
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$ |
(0.40) |
Basic weighted-average shares outstanding |
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45,822,486 |
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35,943,880 |
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Diluted net loss per common share |
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$ |
(0.71) |
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$ |
(0.40) |
Diluted weighted-average shares outstanding |
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45,822,486 |
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35,943,880 |
The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.
4
Senseonics Holdings, Inc.
Unaudited Condensed Consolidated Statements of Changes in Stockholders’ Equity
(in thousands)
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Series B |
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Convertible |
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Accumulated |
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Preferred Stock |
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Common Stock |
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Paid-In |
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Other |
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Accumulated |
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Stockholders' |
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Temporary |
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Shares |
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Amount |
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Capital |
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Comprehensive Loss |
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Deficit |
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Equity |
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Equity |
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Three months ended March 31, 2025: |
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Balance, December 31, 2024 |
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29,767 |
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$ |
30 |
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$ |
931,289 |
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$ |
— |
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$ |
(947,874) |
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$ |
(16,555) |
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$ |
37,656 |
Conversion of preferred stock |
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1,519 |
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2 |
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37,654 |
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— |
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— |
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37,656 |
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(37,656) |
Issuance of common stock, net of issuance costs |
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1,411 |
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1 |
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26,455 |
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— |
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— |
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26,456 |
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— |
Issued common stock for vested RSUs, ESPP purchases and stock option exercises |
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14 |
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— |
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62 |
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— |
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— |
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62 |
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— |
Stock-based compensation expense |
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— |
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— |
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1,840 |
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— |
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— |
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1,840 |
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— |
Net loss |
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— |
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— |
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— |
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— |
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(14,259) |
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(14,259) |
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— |
Other comprehensive loss |
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— |
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— |
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— |
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(3) |
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— |
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(3) |
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— |
Balance, March 31, 2025 |
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32,711 |
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$ |
33 |
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$ |
997,300 |
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$ |
(3) |
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$ |
(962,133) |
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$ |
35,197 |
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$ |
— |
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Three months ended March 31, 2026: |
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Balance, December 31, 2025 |
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41,263 |
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$ |
41 |
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$ |
1,077,923 |
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$ |
69 |
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$ |
(1,016,987) |
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$ |
61,046 |
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$ |
— |
Issuance of common stock, net of issuance costs |
|
478 |
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— |
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3,493 |
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— |
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— |
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3,493 |
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— |
Issued common stock for vested RSUs, ESPP purchases and stock option exercises |
|
73 |
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1 |
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63 |
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— |
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— |
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64 |
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— |
Stock-based compensation expense |
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— |
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— |
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2,276 |
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— |
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— |
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2,276 |
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— |
Shares withheld related to net share settlement of equity awards |
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(19) |
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— |
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(150) |
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— |
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— |
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(150) |
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— |
Net loss |
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— |
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— |
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— |
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— |
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(32,333) |
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(32,333) |
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— |
Other comprehensive loss |
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— |
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— |
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— |
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(61) |
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— |
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(61) |
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— |
Balance, March 31, 2026 |
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41,795 |
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$ |
42 |
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$ |
1,083,605 |
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$ |
8 |
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$ |
(1,049,320) |
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$ |
34,335 |
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$ |
— |
The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.
5
Senseonics Holdings, Inc.
Unaudited Condensed Consolidated Statements of Cash Flows
(in thousands)
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Three Months Ended |
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March 31, |
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2026 |
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2025 |
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Cash flows from operating activities |
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Net loss |
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$ |
(32,333) |
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$ |
(14,259) |
Adjustments to reconcile net loss to net cash used in operating activities: |
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Depreciation and amortization expense |
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545 |
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384 |
Non-cash interest expense (debt discount and deferred costs) |
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325 |
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|
518 |
Net amortization of premiums and accretion of discounts on marketable securities |
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(198) |
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(39) |
Stock-based compensation expense |
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2,276 |
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1,840 |
Provision for inventory obsolescence and losses |
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(345) |
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|
147 |
Allowance for credit losses |
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420 |
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— |
Other |
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4 |
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|
111 |
Changes in assets and liabilities: |
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Accounts receivable |
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(3,010) |
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|
1,650 |
Prepaid expenses and other current assets |
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252 |
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1,033 |
Inventory |
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(1,346) |
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(236) |
Deposits and other assets |
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(301) |
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— |
Accounts payable |
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(870) |
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(852) |
Accrued expenses and other liabilities |
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3,004 |
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(5,655) |
Accrued interest |
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(62) |
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(491) |
Payments on lease liabilities |
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(386) |
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(231) |
Net cash used in operating activities |
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(32,025) |
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(16,080) |
Cash flows from investing activities |
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Capital expenditures |
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(111) |
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(434) |
Purchase of marketable securities |
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(4,042) |
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(24,891) |
Proceeds from sale and maturity of marketable securities |
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23,260 |
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— |
Cash paid in connection with asset acquisition |
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(1,111) |
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— |
Net cash provided by (used in) investing activities |
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17,996 |
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(25,325) |
Cash flows from financing activities |
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Proceeds from issuance of common stock, net |
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3,493 |
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26,456 |
Proceeds from exercise of stock options, RSUs and ESPP issuances, net |
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|
64 |
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62 |
Taxes paid related to net share settlement of equity awards |
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(150) |
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|
— |
Repayment of 2025 Notes |
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— |
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(20,399) |
Net cash provided by financing activities |
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|
3,407 |
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|
6,119 |
Net decrease in cash, cash equivalents, and restricted cash |
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(10,622) |
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|
(35,286) |
Cash, cash equivalents, and restricted cash at beginning of period |
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|
40,549 |
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|
74,912 |
Cash, cash equivalents, and restricted cash at end of period |
|
$ |
29,927 |
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$ |
39,626 |
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|
|
Supplemental disclosure of cash flow information |
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|
Cash paid during the period for interest |
|
$ |
866 |
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$ |
1,402 |
Supplemental disclosure of non-cash investing and financing activities |
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|
|
|
|
Property and equipment purchases included in accounts payable and accrued expenses |
|
|
— |
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|
74 |
Issuance of common stock upon conversion of preferred shares |
|
|
— |
|
|
30,372 |
Lease liabilities arising from obtaining right-of-use assets |
|
|
1,685 |
|
|
— |
Reverse stock split - reclassification from common stock to additional paid-in capital |
|
|
— |
|
|
621 |
The accompanying notes are an integral part of these unaudited condensed consolidated financial statements.
6
Senseonics Holdings, Inc.
Notes to Unaudited Condensed Consolidated Financial Statements
1.Organization and Nature of Operations
Business
Senseonics Holdings, Inc., a Delaware corporation, is a medical technology company focused on the design, development and commercialization of long-term, implantable continuous glucose monitoring (“CGM”) systems to improve the lives of people with diabetes by enhancing their ability to manage their disease with relative ease and accuracy.
Senseonics, Incorporated is a wholly owned subsidiary of Senseonics Holdings, Inc. and was originally incorporated on October 30, 1996, and commenced operations on January 15, 1997. Eon Care Services, LLC and Eon Management Services, LLC are wholly owned subsidiaries of Senseonics, Incorporated formed in April 2024 and July 2024, respectively. In connection with the transition of commercialization activities in Europe, the Company established wholly owned subsidiaries in Italy, Germany, Spain and Sweden in late 2025 and early 2026 to support local commercial operations and distribution activities. Senseonics Holdings, Inc. and its consolidated subsidiaries and affiliated entities, including its consolidated variable interest entities (“VIEs”) are hereinafter collectively referred to as the “Company”, unless otherwise indicated or the context otherwise requires.
Reverse Stock Split
On October 17, 2025, at 4:05 p.m. Eastern Time (the “Effective Time”), the Company effected a 1-for-20 reverse stock split of the Company’s issued and outstanding shares of common stock (the “Reverse Stock Split”) and a proportionate reduction in the total number of authorized shares of its common stock from 1,400,000,000 shares to 70,000,000 shares, as authorized by the Company’s stockholders at the Company’s 2025 special meeting of stockholders held on September 29, 2025 and approved by the Company’s board of directors on October 3, 2025. As a result of the Reverse Stock Split, every 20 shares of issued and outstanding common stock were automatically combined into one issued and outstanding share of common stock, without any change in the par value of $0.001 per share. No fractional shares were issued as a result of the Reverse Stock Split. Stockholders entitled to a fractional share received a cash payment based on the average closing sales price of the Company’s common stock on the NYSE American for the five trading days immediately preceding the Effective Time. All historical share and per share amounts reflected throughout the financial statements have been adjusted to reflect the Reverse Stock Split. Proportionate adjustments were made to the per share exercise price and the number of shares of common stock that may be purchased upon exercise of outstanding stock options and warrants and the number of shares of common stock reserved for future issuance under the Company’s equity compensation plans.
Transfer to Nasdaq Stock Exchange
On November 14, 2025, the Company provided written notice to NYSE American of its determination to make a voluntary withdrawal of the Company’s common stock from the NYSE American to the Nasdaq Global Select Market (“Nasdaq”). The Company ended trading on the NYSE American effective after the market closed on November 14, 2025 and began trading on Nasdaq under the existing ticker symbol “SENS” on November 17, 2025.
2.Liquidity and Capital Resources
The Company has not generated significant profit from the sale of products and its ability to generate revenue and achieve profitability largely depends on the Company’s ability to successfully expand the commercialization of its implantable continuous glucose monitoring systems, including the Eversense E3 system (“Eversense E3”) and the Eversense 365 system (“Eversense 365” and, together with Eversense E3, “Eversense” or the “Eversense Systems”), continue the development of its products and product upgrades, and to obtain necessary regulatory approvals or certifications for the sale of those products. These activities including the costs associated with our plans to transition the commercial activities back to the Company (as further described in Note 4) will require significant uses of working capital through 2026 and beyond.
7
The Company generated total net loss of $(69.1) million and $(78.6) million for the years ended December 31, 2025 and 2024, respectively. For the three months ended March 31, 2026, the Company had a net loss of $32.3 million and an accumulated deficit of $1.0 billion. To date, the Company has funded its operations principally through the issuance of preferred stock, common stock, warrants, convertible notes and debt. As of March 31, 2026, the Company had unrestricted cash, cash equivalents and marketable securities of $64.3 million.
Several actions have been taken by the Company with regards to liquidity and to manage our cash flows for the year ended December 31, 2025, the three months ended March 31, 2026 and subsequent to March 31, 2026. These actions included, but were not limited to, the completion of multiple equity financing transactions during 2025, including an underwritten public offering and private placement resulting in aggregate net proceeds of approximately $72.2 million, approximately $30.8 million in net proceeds received under the Equity Distribution Agreement (as described in Note 13) from March 2024 through March 2025, and approximately $3.5 million in net proceeds from the sale of 478,067 shares under the Sales Agreement (as described in Note 13) during the three months ended March 31, 2026. In addition, subsequent to March 31, 2026, the Company completed additional equity and debt financing transactions as discussed below.
On May 4, 2026, the Company completed an underwritten public offering (the “Public Offering”) of 8,000,000 shares of its common stock at a public offering price of $5.00 per share and, in lieu of common stock, pre-funded warrants to purchase 8,000,000 shares of common stock at a purchase price of $4.999 per pre-funded warrant share. In connection with the offering, the Company granted the underwriters a 30-day option to purchase up to an additional 2,400,000 shares of common stock at the public offering price, less underwriting discounts and commissions, which the underwriters exercised in full. As a result, the total gross proceeds to the Company from the offering were approximately $92.0 million, before deducting underwriting discounts and commissions and other offering expenses payable by the Company. The net proceeds to the Company are estimated to be approximately $86.0 million, after deducting underwriting discounts and commissions and estimated offering expenses. The Public Offering is further described in Note 13.
On May 1, 2026, the Company entered into a Second Amendment to its Loan and Security Agreement with Hercules Capital, Inc. (the “Amended Loan Agreement”), pursuant to which the lenders agreed to make available to the Company up to $140.0 million in senior secured term loans. The facility consists of (i) an initial term loan of $35.0 million, which was previously funded, (ii) an additional term loan of $10.0 million (the “Tranche 2 Loan”), and (iii) additional tranches of term loans in the amounts of up to $10.0 million, $10.0 million, $15.0 million and an uncommitted $60.0 million, respectively, subject to the satisfaction of specified conditions. The loans under the Amended Loan Agreement mature on September 3, 2029. The Second Amendment closed on May 6, 2026 (the “Amendment Closing Date”), and both the 2026 Tranche 2 Loan and 2026 Tranche 3A Loan were funded at closing for total proceeds of $20.0 million. The Amended Loan Agreement is further described in Note 12.
In accordance with the FASB Accounting Standards Codification Topic 205-40, Presentation of Financial Statements- Going Concern, management is required to assess the Company’s ability to continue as a going concern through twelve months after issuance of the financial statements. Management previously disclosed conditions and events that raised substantial doubt about our ability to continue as a going concern. In addition, given the Company’s historical reliance upon debt and equity financing, management will continue to evaluate our funding needs against operating performance and strategic initiatives.
As of the first quarter of 2026, based on current operating plans, the subsequent receipt of financing proceeds, its existing unrestricted cash, cash equivalents and marketable securities, management now believes that the Company has sufficient resources to meet the Company’s anticipated operating needs for the next twelve months from the issuance of the financial statements. Accordingly, management has concluded that the substantial doubt that was raised in the past about the Company’s ability to continue as a going concern has been alleviated.
8
3. |
Summary of Significant Accounting Policies |
Basis of Presentation
The accompanying unaudited condensed consolidated financial statements have been prepared in accordance with U.S. GAAP for interim financial information and the instructions to Quarterly Report on Form 10-Q and Article 10 of Regulation S-X. Although the Company considers the disclosures in these unaudited condensed consolidated financial statements to be adequate to make the information presented not misleading, certain information or footnote information normally included in consolidated financial statements prepared in accordance with U.S. GAAP has been condensed or omitted as permitted under the rules and regulations of the SEC. In the opinion of management, all adjustments (consisting only of normal recurring adjustments) considered necessary for a fair statement of financial position at March 31, 2026, and December 31, 2025, results of operations, comprehensive loss, and changes in stockholders’ equity for the three months ended March 31, 2026 and 2025 and cash flows for the three months ended March 31, 2026 and 2025 have been included. The unaudited condensed consolidated financial statements should be read in conjunction with the Company’s Annual Report on Form 10-K for the year ended December 31, 2025, as filed with the SEC on March 2, 2026. The interim results for March 31, 2026 are not necessarily indicative of the results to be expected for the year ending December 31, 2026, or for any future interim periods.
The consolidated financial statements reflect the accounts of Senseonics Holdings, Inc. and its consolidated subsidiaries and affiliated entities, including its VIEs. All intercompany balances and transactions are eliminated upon consolidation. The Company views its operations and manages its business in one segment, diabetes products and services. Operating segments are defined as components of an enterprise about which separate discrete information is available for evaluation by the chief operating decision maker, or decision-making group, in deciding how to allocate resources and in assessing performance.
In November 2024, Eon Management Services, LLC entered into management services agreements (the “Administrative Agreement”) for an initial fixed term of 10 years with several professional corporations created to support patient access to the Eversense Systems by contracting nurse practitioners and other healthcare professionals to perform Eversense insertion procedures and other clinical activities. On April 1, 2026, Eon Management Services, LLC entered into an additional management services agreement with Meadows Medical Care PC, also with an initial fixed term of 10 years. Eon Care Clinicians PC, Eon Care Clinicians of NJ PC, Eon Care Clinicians of CA PC, and Meadows Medical Care PC (collectively referred to as the “Eon Care PCs”) are professional corporations established pursuant to the requirements of their respective domestic jurisdictions governing the corporate practice of medicine.
In accordance with relevant accounting guidance, the Eon Care PCs have been determined to be VIEs of the Company, as the Company is its primary beneficiary with the ability, through the Administrative Agreement to direct the activities (excluding clinical activities) that most significantly affect the Eon Care PCs financial performance and have the obligation to absorb losses of, or the right to receive benefits from, the Eon Care PCs that could potentially be significant to it. The assets of the consolidated VIEs may only be used to settle obligations of the consolidated VIEs, if any. Our variable interest entities’ assets, liabilities, and results of operations were not material to our consolidated financial results.
Significant Accounting Policies
The accounting policies used by the Company in its presentation of interim financial results are consistent with those presented in Note 3 to the consolidated financial statements included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2025.
Recent Accounting Pronouncements
In November 2024, the FASB issued Accounting Standards Update No. 2024-03, Disaggregation of Income Statement Expenses (DISE) (“ASU 2024-03”), the objective of which is to provide greater transparency about an entity’s expenses to allow investors to better understand an entity’s performance, assessing its prospects for future cash flows, and comparing its performance both over time and with that of other entities. ASU 2024-03 is effective for annual reporting periods beginning after December 15, 2026 and interim reporting periods beginning after December 15, 2027.
9
The requirements will be applied prospectively with the option for retrospective application. Early adoption is permitted. The Company is currently evaluating the impact of the new standard on its financial statements and disclosures.
Use of Estimates
The preparation of consolidated financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and the reported amounts of revenue and expenses during the reporting period. In the accompanying unaudited condensed consolidated financial statements, estimates are used for, but not limited to, stock-based compensation, recoverability of long-lived assets and definite-lived intangible assets, deferred taxes and valuation allowances, fair value of investments, derivative assets and liabilities, obsolete inventory, warranty obligations, variable consideration related to revenue, allowance for credit losses, depreciable lives of property and equipment, amortization periods for identifiable intangible assets, and accruals for clinical study costs, which are accrued based on estimates of work performed under contract. The Company bases these estimates on historical and anticipated results, trends, and various other assumptions that it believes are reasonable, including assumptions as to future events. These estimates form the basis for making judgments about the carrying values of assets and liabilities and recorded revenues and expenses. Actual results could differ from those estimates; however, management does not believe that such differences would be material.
10
4.Revenue Recognition
The Company generates product revenue from sales of the Eversense system and related components and supplies to strategic fulfillment partners and through its consignment network in the United States, as well as to Ascensia Diabetes Care Holdings AG (“Ascensia”) and third-party distributors outside the United States (each, a “Customer” and collectively “Customers”), who then resell the products to health care providers and patients. Effective January 1, 2026, in connection with the parties’ execution of a Master Asset Purchase Agreement on December 31, 2025 (the “Master Asset Purchase Agreement”), the Company reassumed primary commercialization responsibilities in the United States and began marketing and distributing Eversense products through its own sales force and strategic fulfillment partner network. Ascensia continues to support commercialization activities in certain European territories during a defined transition period.
The Company is paid for its sales directly to the Customers, regardless of whether the Customers resell the products to health care providers and patients. The Company also generates product revenue from sales of the Eversense system and related components and supplies through a consignment model with its network of independent healthcare professionals in the United States and revenue is recognized when the product is consumed by a patient. The Company’s policies for recognizing sales have not changed from those described in its Annual Report on Form 10-K for the year ended December 31, 2025.
Revenue by Geographic Region
The following table sets forth net revenue derived from the Company’s two primary geographical markets, the United States and outside of the United States, based on the geographic location to which the Company delivers the product, for the three months ended March 31, 2026 and 2025:
|
|
Three Months Ended |
|
|||
|
|
March 31, 2026 |
|
|||
|
|
|
|
% |
|
|
(Dollars in thousands) |
|
Amount |
|
of Total |
|
|
Revenue, net: |
|
|
|
|
|
|
United States |
|
$ |
9,330 |
|
79.7 |
% |
Outside of the United States |
|
|
2,381 |
|
20.3 |
|
Total |
|
$ |
11,711 |
|
100.0 |
% |
|
|
|
|
|
|
|
|
|
Three Months Ended |
|
|||
|
|
March 31, 2025 |
|
|||
|
|
|
|
% |
|
|
(Dollars in thousands) |
|
Amount |
|
of Total |
|
|
Revenue, net: |
|
|
|
|
|
|
United States |
|
$ |
4,495 |
|
71.8 |
% |
Outside of the United States |
|
|
1,762 |
|
28.2 |
|
Total |
|
$ |
6,257 |
|
100.0 |
% |
Contract Assets
Contract assets consist of unbilled receivables from Customers and are recorded at net realizable value. Included in accounts receivable, net as of March 31, 2026 and December 31, 2025 are unbilled accounts receivable of less than $0.1 million and $2.1 million, respectively, which are related to the timing of billings. Included in accounts receivable – related parties, net are unbilled accounts receivable of $2.3 million and $2.0 million for the periods ended March 31, 2026 and December 31, 2025, respectively, which are related to revenue share variable consideration from the Commercialization Agreement. The Company expects to invoice and collect all unbilled accounts receivable within twelve months.
11
Concentration of Revenue and Customers
A significant portion of the Company’s revenue is derived from one Customer, Ascensia. For the three months ended March 31, 2026 and 2025, sales to Ascensia accounted for 20% and 71% of total revenue, respectively.
A portion of the Company’s revenue is earned via consignment arrangements with healthcare providers. For the three months ended March 31, 2026 and 2025, sales under consignment arrangements accounted for 37.3% and 19.6% of total revenue, respectively. During 2025, Ascensia earned commissions on sales made through these consignment arrangements for the support provided by their sales reps and commercial organization. Revenues for these corresponding periods represent sales of sensors, transmitters and miscellaneous Eversense System components.
Termination and Modification of Commercialization Arrangements
On September 3, 2025, the Company and Ascensia entered into a memorandum of understanding related to the transition of commercial operations for Eversense from Ascensia back to the Company. On December 31, 2025, the parties executed a Master Asset Purchase Agreement and effective January 1, 2026 the parties entered into an Amended and Restated Collaboration and Commercialization Agreement (the “A&R Commercialization Agreement”), which terminated Ascensia’s rights to market Eversense products in the United States and made Ascensia’s European commercialization rights non-exclusive.
Following the A&R Commercialization Agreement, Ascensia has no further rights to revenues from sales of Eversense products in the United States, and effective January 1, 2026, the Company is entitled to 100% of revenues from sales in Italy, Germany, Spain and Sweden (the “European Territories”), subject to transitional arrangements. In connection with the transition of U.S. commercialization activities, the Company entered into agreements with certain U.S. strategic fulfillment partners that previously distributed products on behalf of Ascensia, consistent with the Company’s historical distribution relationships.
As a result of the termination and modification of the arrangement, the Company reassessed its remaining performance obligations and adjusted related contract assets and contract liabilities in accordance with ASC 606. In connection with the termination, the Company accepted the return of certain unsold inventory previously held by Ascensia, reversed $0.4 million of revenue, and recorded the returned inventory at its estimated net realizable value as of December 31, 2025.
Additional information regarding the Master Asset Purchase Agreement and related transactions is included in Note 17 — Related Party Transactions.
5.Net Loss per Share
Basic net loss per share attributable to common stockholders is calculated by dividing the net loss attributable to common stockholders by the weighted-average number of common shares outstanding during the period. An aggregate of 4,197,554 shares of common stock issuable upon the exercise of the PHC Exchange Warrant (as defined below) and the Purchase Warrant (as defined below) held by PHC Holdings Corporation, the parent company of Ascensia (“PHC”) are included in the number of outstanding shares used for the computation of basic net loss per share for the three months ended March 31, 2026 and 2025. Since the shares are issuable for little or no consideration, sometimes referred to as “penny warrants”, they are considered outstanding in the context of earnings per share, as discussed in ASC 260-10-45-13.
Diluted net loss per share is computed using the weighted average number of common shares outstanding during the period and, when dilutive, potential common share equivalents. Potentially dilutive common shares consist of shares issuable from restricted stock units (“RSUs”), stock options, warrants and the Company’s convertible notes. Potentially dilutive common shares issuable upon vesting of restricted stock units, exercise of stock options and exercise of warrants are determined using the average share price for each period under the treasury stock method. Potentially dilutive common shares issuable upon conversion of the Company’s convertible notes are determined using the if-converted method. The if-converted method assumes conversion of convertible securities at the beginning of the reporting period.
12
Interest expense, dividends, and the changes in fair value measurement recognized during the period are added back to the numerator. The denominator includes the common shares issuable upon conversion of convertible securities.
In periods of net loss, all potentially dilutive common shares are excluded from the computation of the diluted net loss per share for those periods, as the effect would be anti-dilutive.
The following table sets forth the computation of basic and diluted net loss per share for the periods shown:
(Dollars, in thousands, except per share amounts)
|
|
Three Months Ended March 31, |
||||
|
|
2026 |
|
2025 |
||
Net loss |
|
$ |
(32,333) |
|
$ |
(14,259) |
Basic weighted average common shares outstanding |
|
|
45,822,486 |
|
|
35,943,880 |
Net loss per share: |
|
|
|
|
|
|
Basic and diluted |
|
$ |
(0.71) |
|
$ |
(0.40) |
Outstanding anti-dilutive securities not included in the diluted net loss per share calculations were as follows:
|
|
Three Months Ended March 31, |
||||
|
|
2026 |
|
2025 |
||
Stock-based awards |
|
|
2,668,604 |
|
|
1,887,857 |
Warrants |
|
|
2,357,747 |
|
|
2,357,747 |
Total anti-dilutive shares outstanding |
|
|
5,026,351 |
|
|
4,245,604 |
6. |
Composition of Certain Financial Statement Items |
Cash, Cash Equivalents, and Restricted Cash
Cash, cash equivalents, and restricted cash consisted of the following (in thousands):
|
|
March 31, |
|
December 31, |
||
|
|
2026 |
|
2025 |
||
Cash |
|
$ |
7,794 |
|
$ |
6,610 |
Money market funds |
|
|
21,818 |
|
|
33,624 |
Restricted Cash |
|
|
315 |
|
|
315 |
Total cash, cash equivalents, and restricted cash |
|
$ |
29,927 |
|
$ |
40,549 |
The Company’s restricted cash relates to collateral for procurement cards issued by a U.S. commercial bank.
Accounts receivable, net
Accounts receivable, net consisted of the following (in thousands):
|
|
March 31, |
|
December 31, |
||
|
|
2026 |
|
2025 |
||
Accounts receivable |
|
$ |
12,335 |
|
$ |
8,067 |
Accounts receivable - related parties |
|
|
4,056 |
|
|
5,312 |
Less: allowance for credit losses |
|
|
(1,680) |
|
|
(1,260) |
Total accounts receivable, net |
|
$ |
14,711 |
|
$ |
12,119 |
13
Inventory, net
Inventory, net of reserves, consisted of the following (in thousands):
|
|
March 31, |
|
December 31, |
||
|
|
2026 |
|
2025 |
||
Finished goods |
|
$ |
3,472 |
|
$ |
2,580 |
Work-in-process |
|
|
4,379 |
|
|
3,631 |
Raw materials |
|
|
457 |
|
|
492 |
Total |
|
$ |
8,308 |
|
$ |
6,703 |
The Company charged $0.1 million in cost of sales for the three months ended March 31, 2026 and $0.7 million in cost of sales for the year ended December 31, 2025 to reduce the value of inventory for items that are potentially obsolete due to expiry, in excess of product demand, or to adjust costs to their net realizable value.
Property, equipment and intangible assets, net
Property, equipment and intangible assets, net, consisted of the following (in thousands):
|
|
March 31, |
|
December 31, |
||
|
|
2026 |
|
2025 |
||
Property and equipment |
|
|
|
|
|
|
Machinery and laboratory equipment |
|
$ |
4,006 |
|
$ |
3,904 |
Office furniture and equipment |
|
|
611 |
|
|
611 |
Leasehold improvements |
|
|
2,209 |
|
|
2,200 |
Intangible assets |
|
|
|
|
|
|
Sensor insertion network assets |
|
|
800 |
|
|
800 |
Less: Accumulated depreciation and amortization |
|
|
(3,479) |
|
|
(3,315) |
Property, equipment and intangible assets, net |
|
$ |
4,147 |
|
$ |
4,200 |
7. |
Marketable Securities |
Marketable securities available for sale were as follows (in thousands):
|
|
March 31, 2026 |
||||||||||
|
|
|
|
Gross |
|
Gross |
|
Estimated |
||||
|
|
Amortized |
|
Unrealized |
|
Unrealized |
|
Market |
||||
|
|
Cost |
|
Gains |
|
Losses |
|
Value |
||||
Commercial Paper |
|
$ |
1,680 |
|
$ |
— |
|
$ |
(1) |
|
$ |
1,679 |
Corporate debt securities |
|
|
12,484 |
|
|
2 |
|
|
(3) |
|
|
12,483 |
Government and agency securities |
|
|
20,542 |
|
|
5 |
|
|
— |
|
|
20,547 |
Total |
|
$ |
34,706 |
|
$ |
7 |
|
$ |
(4) |
|
$ |
34,709 |
|
|
December 31, 2025 |
||||||||||
|
|
|
|
Gross |
|
Gross |
|
Estimated |
||||
|
|
Amortized |
|
Unrealized |
|
Unrealized |
|
Market |
||||
|
|
Cost |
|
Gains |
|
Losses |
|
Value |
||||
Commercial Paper |
|
$ |
6,396 |
|
$ |
3 |
|
$ |
— |
|
$ |
6,399 |
Corporate debt securities |
|
|
12,452 |
|
|
18 |
|
|
— |
|
|
12,470 |
Government and agency securities |
|
|
34,879 |
|
|
48 |
|
|
— |
|
|
34,927 |
Total |
|
$ |
53,727 |
|
$ |
69 |
|
$ |
— |
|
$ |
53,796 |
14
The following are the scheduled maturities as of March 31, 2026 (in thousands):
|
|
Net |
|
Fair |
||
|
|
Carrying Amount |
|
Value |
||
2026 (remaining nine months) |
|
$ |
34,706 |
|
$ |
34,709 |
Thereafter |
|
|
— |
|
|
— |
Total |
|
$ |
34,706 |
|
$ |
34,709 |
The Company periodically reviews its portfolio of debt securities to determine if any investment is impaired due to credit loss or other potential valuation concerns. For debt securities where the fair value of the investment is less than the amortized cost basis, the Company assesses at the individual security level, for various quantitative factors including, but not limited to, the nature of the investments, changes in credit ratings, interest rate fluctuations, industry analyst reports, and the severity of impairment. Unrealized losses on available-for-sale securities at March 31, 2026 were not significant and were primarily due to changes in interest rates and not due to increased credit risk associated with specific securities. The Company does not intend to sell these impaired investments and it is not more likely than not that the Company will be required to sell the investments before recovery of their amortized cost bases, which may be at maturity.
8. |
Prepaid Expenses and Other Current Assets |
Prepaid expenses and other current assets consisted of the following (in thousands):
|
|
March 31, |
|
December 31, |
||
|
|
2026 |
|
2025 |
||
Contract manufacturing(1) |
|
$ |
2,445 |
|
$ |
1,949 |
Clinical and Preclinical |
|
|
848 |
|
|
883 |
Interest receivable |
|
|
341 |
|
|
311 |
Sales and marketing |
|
|
330 |
|
|
492 |
IT and software |
|
|
214 |
|
|
310 |
Other |
|
|
448 |
|
|
421 |
Total prepaid expenses and other current assets |
|
$ |
4,626 |
|
$ |
4,366 |
| (1) | Includes deposits to contract manufacturers for manufacturing process. |
9. |
Accrued Expenses and Other Current Liabilities |
Accrued expenses and other current liabilities consisted of the following (in thousands):
|
|
March 31, |
|
December 31, |
||
|
|
2026 |
|
2025 |
||
Sales and marketing services |
|
$ |
8,592 |
|
$ |
5,028 |
Professional and administrative services |
|
|
4,647 |
|
|
3,784 |
Compensation and benefits |
|
|
3,214 |
|
|
5,271 |
Research and development |
|
|
2,187 |
|
|
2,705 |
Patient access and incentive programs |
|
|
1,667 |
|
|
— |
Contract manufacturing |
|
|
1,214 |
|
|
1,673 |
Operating lease |
|
|
944 |
|
|
496 |
Other |
|
|
672 |
|
|
1,332 |
Total accrued expenses and other current liabilities |
|
$ |
23,137 |
|
$ |
20,289 |
15
10. |
Leases |
The Company leases approximately 33,000 square feet of research and office space for its corporate
headquarters under a non-cancelable operating lease. The Company has one option to extend the term for an additional period of five years beginning on June 1, 2033.
In addition, effective January 1, 2026, in connection with the acquisition of certain U.S. commercial assets under the Master Asset Purchase Agreement with Ascensia, the Company assumed operating leases for a fleet of vehicles used by its U.S. sales force. These leases are classified as operating leases and have remaining lease terms with expirations ranging from May 31, 2028 to June 30, 2030.
The rent expense is recognized on a straight-line basis through the end of the lease term, excluding option renewals. The difference between the straight-line rent amounts and amounts payable under the lease is recorded as deferred lease cost.
Operating lease expense was $0.4 million and $0.2 million for the three months ended March 31, 2026 and 2025.
The following table summarizes the lease assets and liabilities as of March 31, 2026 and December 31, 2025 (in thousands):
|
|
|
|
|
March 31, |
|
December 31, |
||
Operating Lease Assets and Liabilities |
|
Balance Sheet Classification |
|
2026 |
|
2025 |
|||
Assets |
|
|
|
|
|
|
|
|
|
Operating lease ROU assets |
|
Deposits and other assets |
|
$ |
6,053 |
|
$ |
4,460 |
|
Liabilities |
|
|
|
|
|
|
|
|
|
Current operating lease liabilities |
|
Accrued expenses and other current liabilities |
|
$ |
944 |
|
$ |
496 |
|
Non-current operating lease liabilities |
|
Non-current operating lease liabilities |
|
|
6,285 |
|
|
5,289 |
|
Total operating lease liabilities |
|
|
|
|
$ |
7,229 |
|
$ |
5,785 |
The following table summarizes the maturity of undiscounted payments due under operating lease liabilities and the present value of those liabilities as of March 31, 2026 (in thousands):
2026 (remaining 9 months) |
|
$ |
1,269 |
2027 |
|
|
1,685 |
2028 |
|
|
1,649 |
2029 |
|
|
1,346 |
2030 |
|
|
1,148 |
Thereafter |
|
|
2,763 |
Total |
|
|
9,860 |
Less: Present value adjustment |
|
|
(2,631) |
Present value of lease liabilities |
|
$ |
7,229 |
The following table summarizes the weighted-average lease term and weighted-average discount rate as of March 31, 2026:
Remaining lease term (years) |
|
2026 |
|
Operating leases |
|
6.5 |
|
Discount rate |
|
|
|
Operating leases |
|
9.4 |
% |
|
|
|
|
16
11. |
Product Warranty Obligations |
The Company provides a warranty of one year on its smart transmitters. Additionally, the Company may also replace Eversense system components that do not function in accordance with the product specifications. Estimated replacement costs are recorded at the time of shipment as a charge to cost of sales in the consolidated statement of operations and are developed by analyzing product performance data and historical replacement experience, including comparing actual return management authorizations to revenue.
The following table provides a reconciliation of the change in estimated warranty liabilities for the three months ended March 31, 2026, and for the twelve months ended December 31, 2025 (in thousands):
|
|
March 31, |
|
December 31, |
||
|
|
2026 |
|
2025 |
||
Balance at beginning of the period |
|
$ |
448 |
|
$ |
406 |
Provision for warranties during the period |
|
|
74 |
|
|
408 |
Settlements made during the period |
|
|
(192) |
|
|
(366) |
Balance at end of the period |
|
$ |
330 |
|
$ |
448 |
12. |
Notes Payable, Preferred Stock and Stock Purchase Warrants |
Term Loans
Loan and Security Agreement
On September 8, 2023 (the “Effective Date”), the Company entered into a loan agreement (the “Loan and Security Agreement”) with Hercules Capital, Inc. and its managed fund (collectively, the “Lenders”), pursuant to which the Lenders agreed to make available to Senseonics up to $50.0 million in senior secured term loans (the “Term Loan Facility”), consisting of (i) an initial term loan of $25.0 million, which was funded on the Effective Date, (ii) $10.0 million, which was funded on January 2, 2024 upon meeting certain terms and conditions under the loan agreement, and (iii) $15.0 million which has not been drawn. On September 3, 2025 (the “2025 Effective Date”), the Company entered into the Amended Loan and Security Agreement with the Lenders and Hercules. The Amended Loan and Security Agreement increased the total loan commitment under the facility from $50.0 million to $100.0 million (collectively, the “2025 Term Loans”). In the Amended Loan and Security Agreement, the undrawn loans increased from $15.0 million to $65.0 million divided into three tranches of up to $10.0 million (“2025 Tranche 2 Loan”), up to $20.0 million (“2025 Tranche 3 Loan”) and up to $35.0 million (“2025 Tranche 4 Loan”), respectively, each of which will become available to Senseonics upon Senseonics’ satisfaction of certain terms and conditions set forth in the Amended Loan and Security Agreement. The loans under the Amended Loan and Security Agreement mature on September 3, 2029 (the “Maturity Date”).
The loans under the Amended Loan and Security Agreement bear interest at an annual rate equal to the greater of (i) the prime rate as reported in The Wall Street Journal plus 2.40% and (ii) 9.90%. Borrowings under the Amended Loan and Security Agreement are repayable in monthly interest-only payments through October 1, 2027. The interest-only period will be extended through October 2, 2028 if the Company satisfies the conditions for the 2025 Tranche 2 Loan, and through the maturity date of the loan if the Company satisfies the conditions for both the 2025 Tranche 2 Loan and 2025 Tranche 3 Loan. After the interest-only payment period, borrowings under the Amended Loan and Security Agreement are repayable in equal monthly payments of principal and accrued interest until the Maturity Date.
At the Company’s option, the Company may prepay all or any portion of the outstanding borrowings under the Amended Loan and Security Agreement, subject to a prepayment fee equal to (a) 3.0% of the principal amount being prepaid if the prepayment occurs within one year of the 2025 Effective Date, 2.0% of the principal amount being prepaid if the prepayment occurs during the second year following the 2025 Effective Date, and 1.00% of the principal amount being prepaid if the prepayment occurs more than two years after the 2025 Effective Date and prior to the Maturity Date.
17
In addition, the Company paid $425,000 in facility fees upon drawing Tranche 1 Loan and Tranche 2 Loan and additional facility fees of $412,500 upon execution of the Amended Loan and Security Agreement. The Company will pay additional facility charges in connection with any borrowing of the 2025 Term Loans, in the amount of 0.50% of the 2025 Tranche 2 Loan and 2025 Tranche 3 Loan and 1.00% of the 2025 Tranche 4 Loan. The Amended Loan and Security Agreement also provides for an end of term fee in an amount equal to 6.45% of the aggregate principal advances of the 2025 Term Loans, which fee is due and payable on the earliest to occur of (i) the Maturity Date, (ii) the date the Company prepays the outstanding loans in full, and (iii) the date that the secured obligations become due and payable. The existing end of term fee under the existing Tranche 1 Loan and Tranche 2 Loan remains payable on September 1, 2027 (the original maturity date). The end of term fees are accreted to interest expense over the term of the loans.
The Company’s obligations under the Amended Loan and Security Agreement are secured by a first-priority security interest in substantially all of its assets. The Amended Loan and Security Agreement contains a minimum cash covenant that requires the Company to hold unrestricted cash equal to 80% of the total amounts funded under the Amended Loan and Security Agreement, reduced to 55% and 35% subject to achieving certain milestones under the agreement. The Amended Loan and Security Agreement also contains a performance covenant that commenced on January 1, 2026, that requires the Company to achieve certain net product revenue targets on a trailing six-month basis for applicable measuring periods. The performance covenant shall be waived at any time in which either (a) the Company’s market capitalization exceeds $550.0 million and the Company maintains unrestricted cash equal to at least 75% of the total amounts funded, or (b) the Company maintains unrestricted cash equal to at least 100% of the total amounts funded.
In addition, the Amended Loan and Security Agreement contains customary representations and warranties and customary affirmative and negative covenants, including, among other things, restrictions on indebtedness, liens, investments, mergers, corporate changes, dispositions, prepayment of other indebtedness, and dividends and other distributions, subject to certain exceptions. The Amended Loan and Security Agreement also contains events of default including, among other things, payment defaults, breach of covenants, material adverse effect, breach of representations and warranties, cross-default to material indebtedness, bankruptcy-related defaults, judgment defaults, revocation of certain government approvals, and the occurrence of certain adverse events. Following an event of default and any applicable cure period, a default interest rate equal to the then-applicable interest rate plus 4.0% may be applied to the outstanding amount, and the Lenders will have the right to accelerate all amounts outstanding under the Loan and Security Agreement, in addition to other remedies available to them as secured creditors of the Company. The Company was in compliance with all covenants as of March 31, 2026.
In addition, in connection with the issuance of the Tranche 1 Loan, the Company issued warrants to the Lenders (collectively, the “Tranche 1 Warrants”) to acquire an aggregate of 41,619 shares of the Company’s common stock at an exercise price of $12.01 per share (the “Tranche 1 Warrant Shares”). For the Tranche 2 Loan the Company issued additional warrants to the Lenders (collectively, the “Tranche 2 Warrants”) to acquire an aggregate of 17,395 shares at an exercise price of $11.50 per share (the “Tranche 2 Warrant Shares”). On the 2025 Effective date, the exercise price of all outstanding warrants was reduced to $9.09 per share (the “Amended Exercise Price”). The Tranche 1 Warrant Shares and Tranche 2 Warrant Shares may be exercised through the earlier of (i) the seventh anniversary of the initial issuance date and (ii) the consummation of certain acquisition transactions involving the Company, as set forth in the Warrants. The number of Tranche 1 Warrant Shares and Tranche 2 Warrant Shares for which the Tranche 1 Warrants and Tranche 2 Warrants are exercisable, and the associated exercise price are subject to certain customary proportional adjustments for fundamental events, including stock splits and reverse stock splits, as set forth in the Warrants. The proceeds from the Loan and Security Agreement were allocated between the Tranche 1 Loan and the Tranche 1 Warrants based on their respective fair value of $25.0 million and $0.4 million, and the amount allocated to the Tranche 1 Warrants was recorded in equity resulting in a debt discount to the Tranche 1 Loan. The Company estimated the fair value of the Tranche 2 Warrants as of the grant date to be $0.1 million and classified the full amount in equity. As a result of the Amended Exercise Price, the value of all outstanding warrants was reduced by $0.2 million. The value of the warrants are amortized as additional interest expense over the term of the Amended Loan and Security Agreement using the effective interest method.
18
In connection with Loan and Security Agreement, the Company incurred $1.1 million in debt issuance costs and debt discounts which are netted against the principal balance of the initial term loan and amortized as interest expense over the term of the loan. The Company incurred additional debt discounts of $0.2 million under the Amended Loan and Security Agreement. The Company evaluated Amended Loan and Security Agreement in accordance with ASC 470-50, Debt, and determined that the amendment resulted in a debt modification. Therefore, no loss on debt extinguishment was recognized. The unamortized debt issuance costs and debt discounts are amortized over the revised term of the loan using an effective interest rate of 13.10%.
Pursuant to the Amended Loan and Security Agreement, the Company also agreed to issue additional seven year term warrants upon the funding of the 2025 Tranche 2 Loan, 2025 Tranche 3 Loan, and 2025 Tranche 4 Loan which warrants would be exercisable for an aggregate number of shares equal to 2.0% of the funded loan amount divided by the exercise price equal to the three-day volume-weighted average price at the time of each advance.
Subsequent to March 31, 2026, on May 6, 2026, the Company entered into a Second Amendment to the Amended Loan and Security Agreement, which increased the total loan commitment up to $140.0 million. See Note 19 for additional information.
Convertible Notes
2025 Notes
In July 2019, the Company issued $82.0 million in aggregate principal amount of senior convertible notes due January 15, 2025 (the “2025 Notes”).
Over the term of the 2025 Notes, the Company completed a series of exchanges and conversions that reduced the outstanding principal balance, including (i) the settlement of $24.0 million aggregate principal in April 2020 pursuant to an exchange agreement (ii) conversions of $6.8 million aggregate principal into shares of common stock between September 2020 and January 2021, and (iii) privately negotiated exchange transactions in August and September 2023 under which $30.8 million aggregate principal was exchanged for a combination of cash and shares of common stock.
Following these transactions, approximately $20.4 million aggregate principal amount of the 2025 Notes remained outstanding. On January 15, 2025, the Company repaid the outstanding principal and accrued interest for the 2025 Notes in the full amount of $20.9 million.
The following carrying amounts are outstanding under the Company’s notes payable as of March 31, 2026 and December 31, 2025 (in thousands):
|
March 31, 2026 |
||||||
|
Principal ($) |
|
Debt (Discount) Premium ($)⁽¹⁾ |
|
Issuance Costs ($) |
|
Carrying Amount ($) |
Amended Loan and Security Agreement |
35,000 |
|
1,065 |
|
(153) |
|
35,912 |
|
|
|
|
|
|
|
|
|
December 31, 2025 |
||||||
|
Principal ($) |
|
Debt (Discount) Premium ($)⁽¹⁾ |
|
Issuance Costs ($) |
|
Carrying Amount ($) |
Amended Loan and Security Agreement |
35,000 |
|
753 |
|
(167) |
|
35,586 |
|
|
|
|
|
|
|
|
| (1) | Includes accretion of end of term fees payable at maturity |
19
Interest expense related to the notes payable for the periods presented below is as follows (in thousands):
|
Three Months Ended March 31, 2026 |
||||||||
|
Interest Rate |
|
Interest ($) |
|
Debt Discount and Fees ($)⁽¹⁾ |
|
Issuance Costs ($) |
|
Total Interest Expense ($) |
Amended Loan and Security Agreement |
9.90% |
|
867 |
|
312 |
|
13 |
|
1,192 |
Total |
|
|
867 |
|
312 |
|
13 |
|
1,192 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Three Months Ended March 31, 2025 |
||||||||
|
Interest Rate |
|
Interest ($) |
|
Debt Discount and Fees ($)⁽¹⁾ |
|
Issuance Costs ($) |
|
Total Interest Expense ($) |
2025 Notes |
5.25% |
|
45 |
|
256 |
|
5 |
|
306 |
Loan and Security Agreement |
9.90% |
|
866 |
|
234 |
|
23 |
|
1,123 |
Total |
|
|
911 |
|
490 |
|
28 |
|
1,429 |
The following are the scheduled maturities of the Company’s notes payable (including end of term fees) as of March 31, 2026 (in thousands):
2027 |
|
$ |
6,622 |
2028 |
|
|
17,829 |
2029 |
|
|
15,239 |
Total |
|
$ |
39,690 |
13. |
Stockholders’ Equity |
Public and Registered Direct Offerings
On May 15, 2025, the Company entered into an underwriting agreement (the “Underwriting Agreement”) with several underwriters for the sale of 5,000,000 shares of its common stock (the “Public Offering”), at a public offering price of $10.00 per share (the “Public Offering Price”). Under the terms of the Underwriting Agreement, the Company also granted the underwriters a 30-day option to purchase up to an additional 750,000 shares of common stock at the Public Offering Price, which the underwriters exercised in full. The Company received aggregate gross proceeds from the Public Offering of $57.5 million. The Company also entered into a securities purchase agreement with Abbott Laboratories (“Abbott”) pursuant to which the Company agreed to issue and sell 2,026,963 shares of its common stock substantially concurrently with the Public Offering, at the Public Offering Price, to Abbott for an aggregate purchase price of approximately $20.3 million in a private placement (the “Private Placement”). The Public Offering and Private Placement closed on May 19, 2025 and May 20, 2025, respectively, and the Company received net proceeds of approximately $52.1 million and $20.1 million, respectively, after deducting underwriting discount, commissions, and offering expenses.
Subsequent to March 31, 2026, on May 4, 2026, the Company completed the May 2026 Offering (as defined below) of 8,000,000 shares of its common stock at a public offering price of $5.00 per share and, in lieu of common stock, May 2026 Pre-Funded Warrants (as defined below) to purchase 8,000,000 shares of common stock at a purchase price of $4.999 per May 2026 Pre-Funded Warrant share. In connection with the offering, the Company granted the underwriters a 30-day option to purchase up to an additional 2,400,000 shares of common stock at the public offering price which was exercised in full. As a result, the Company issued a total of 18,400,000 shares of common stock and pre-funded warrants and received gross proceeds of approximately $92.0 million, before deducting underwriting discounts, commissions and offering expenses.
ATM Offerings
On August 6, 2025, the Company entered into an at-the-market sales agreement (the “Sales Agreement”) with TD Securities (USA) LLC (“TD Cowen”), under which the Company could offer and sell, from time to time, at its sole discretion, shares of its common stock having an aggregate offering price of up to $100.0 million through TD Cowen as its sales agent in an “at the market” offering, or ATM offering. TD Cowen will receive commissions up to 3.0% of the gross proceeds of any common stock sold through TD Cowen under the Sales Agreement.
20
The shares were offered and sold pursuant to an effective shelf registration statement on Form S-3, which was originally filed with the Securities and Exchange Commission on August 6, 2025. During the three months ended March 31, 2026, the Company received approximately $3.5 million in proceeds from the sale of 478,067 shares under the Sales Agreement, after deducting sales commissions and offering expenses.
In August 2023, the Company entered into an Equity Distribution Agreement (the “Equity Distribution Agreement”) with Goldman Sachs & Co. LLC (“GS”), under which the Company could offer and sell, from time to time, at its sole discretion, shares of its common stock having an aggregate offering price of up to $106.6 million through GS as its sales agent in an “at the market” offering. GS received commissions up to 3.0% of the gross proceeds of any common stock sold through GS under the Equity Distribution Agreement. The shares were offered and sold pursuant to an effective shelf registration statement on Form S-3, which was originally filed with the Securities and Exchange Commission on August 10, 2023. On October 24, 2024, the Company amended the Equity Distribution Agreement with GS to reduce the maximum amount of shares issuable thereunder to $55.0 million. On May 15, 2025, in connection with the Public Offering and Private Placement, the Equity Distribution Agreement was terminated. At the time of termination of the Equity Distribution Agreement on May 15, 2025, the Company had received approximately $30.8 million in net proceeds from the sale of 2,006,528 shares under the Equity Distribution Agreement, after deducting sales commissions and offering expenses.
Stock Purchase Warrants
The table below summarizes the warrant activity for the three months ended March 31, 2026 (in thousands). This table does not include the PHC Exchange Warrant (as defined below) or the PHC Purchase Warrant (as defined and described below). Such warrants are pre-funded and excluded from the table due to their nominal exercise price of $0.02 per warrant share.
|
|
Shares |
|
Exercise price (per share) |
|
Weighted average exercise price (per share) |
||
Outstanding, December 31, 2025 |
|
2,357,747 |
|
$ |
7.00 to 77.20 |
|
$ |
7.40 |
Granted |
|
— |
|
|
— |
|
|
— |
Exercised |
|
— |
|
|
— |
|
|
— |
Expired |
|
— |
|
|
— |
|
|
— |
Outstanding and Exercisable, March 31, 2026 |
|
2,357,747 |
|
$ |
7.00 to 77.20 |
|
$ |
7.40 |
|
|
|
|
|
|
|
|
|
Weighted Average Remaining Life, March 31, 2026 (years) |
|
4.07 |
|
|
|
|
|
|
On June 30, 2016, we entered into a loan agreement with Oxford Finance and Silicon Valley Bank (collectively, the “Lenders”) and issued to the Lenders 10-year stock purchase warrants to purchase an aggregate of 5,830, 3,152 and 4,033 shares of common stock at an exercise price of $77.20, $47.60 and $37.20 per share, respectively (“Oxford/SVB Warrants”). The Oxford/SVB Warrants expire on June 30, 2026, November 22, 2026 and March 29, 2027, respectively.
On March 13, 2023, we issued and sold to PHC a warrant to purchase 771,288 shares of common stock for $15.0 million (the “Purchase Warrant”). The Purchase Warrant is a “pre-funded” warrant with a nominal exercise price of $0.02 per share. All or any part of the Purchase Warrant is exercisable by PHC at any time and from time to time.
In March 2023, we entered into an exchange agreement with PHC, pursuant to which PHC exchanged $35.0 million aggregate principal amount of convertible notes due October 31, 2024, including all accrued and unpaid interest thereon, for a warrant (the “PHC Exchange Warrant”) to purchase up to 3,426,266 shares of common stock (the “PHC Exchange Warrant Shares”). The PHC Exchange Warrant is a “pre-funded” warrant with a nominal exercise price of $0.02 per PHC Exchange Warrant Share. All or any part of the PHC Exchange Warrant is exercisable by PHC at any time and from time to time.
21
On September 8, 2023, we entered into the Loan and Security Agreement with several lenders and issued the Tranche 1 Warrants to acquire an aggregate of 41,619 shares of common stock at an initial exercise price of $12.01 per share. The Tranche 1 Warrants may be exercised through the earlier of (i) September 8, 2030 and (ii) the consummation of certain acquisition transactions involving the company, as set forth in the warrant agreement. On September 3, 2025, the Company and the lenders entered into an amendment to reduce the exercise price to $9.09 per share. All other terms of the warrants, including the expiration date and number of shares issuable upon exercise, remain unchanged.
On January 2, 2024, we issued the Tranche 2 Warrants to acquire an aggregate of 17,395 shares at an initial exercise price of $11.50 per share. The Tranche 2 Warrants may be exercised through the earlier of (i) January 2, 2031 and (ii) the consummation of certain acquisition transactions involving the company, as set forth in the warrant agreement. On September 3, 2025, the Company and the lenders entered into an amendment to reduce the exercise price to $9.09 per share. All other terms of the warrants, including the expiration date and number of shares issuable upon exercise, remain unchanged.
On October 24, 2024, in connection with a registered direct securities offering, the Company issued to the investors in the offering warrants to purchase an aggregate of 2,285,714 shares of common stock at an exercise price of $7.00 per share. The warrants were non-exercisable for the first six months after issuance and expire on April 29, 2030.
14. |
Stock-Based Compensation |
2015 Plan
In December 2015, the Company adopted the 2015 Equity Incentive Plan (the “2015 Plan”), under which incentive stock options, non-qualified stock options and restricted stock units may be granted to the Company’s employees and certain other persons, such as officers and directors, in accordance with the 2015 Plan provisions. In February 2016, the Company’s Board of Directors adopted, and the Company’s stockholders approved, an Amended and Restated 2015 Equity Incentive Plan (the “Amended and Restated 2015 Plan”), which became effective on February 20, 2016. The Company’s Board of Directors may terminate the Amended and Restated 2015 Plan at any time. Options granted under the Amended and Restated 2015 Plan expire ten years after the date of grant.
Pursuant to the Amended and Restated 2015 Plan, the number of shares of the Company’s common stock reserved for issuance automatically increases on January 1 of each year, ending on January 1, 2026, by 3.5% of the total number of shares of its common stock outstanding on December 31 of the preceding calendar year, or a lesser number of shares as may be determined by its Board of Directors. As of March 31, 2026, 3,009,371 shares remained available for grant under the Amended and Restated 2015 Plan.
Inducement Plan
On May 30, 2019, the Company adopted the Senseonics Holdings, Inc. Inducement Plan (the “Inducement Plan”), pursuant to which the Company reserved 90,000 shares of the Company’s common stock for issuance. The only persons eligible to receive grants of awards under the Inducement Plan are individuals who satisfy the standards for inducement grants in accordance with Nasdaq Listing Rule 5635(c)(4), including individuals who were not previously an employee or director of the Company, or following a bona fide period of non-employment, as an inducement material to such persons entering into employment with the Company. An “Award” is any right to receive the Company’s common stock pursuant to the Inducement Plan, consisting of non-statutory options, restricted stock unit awards and other equity incentive awards. As of March 31, 2026, 27,406 shares remained available for grant under the Inducement Plan.
Commercial Equity Plan
On January 30, 2023, the Company adopted the Senseonics Holdings, Inc. 2023 Commercial Equity Plan (the “Commercial Equity Plan”), pursuant to which the Company reserved 500,000 shares of common stock for issuance. Eligible recipients under the plan are non-employees of Senseonics who assist with the commercialization of Eversense. An “Award” is any right to receive the Company’s common stock pursuant to the Commercial Equity Plan, consisting of non-statutory options and restricted stock unit awards.
22
As of March 31, 2026, 165,753 shares remained available for grant under the Commercial Equity Plan.
2016 Employee Stock Purchase Plan
In February 2016, the Company adopted the 2016 Employee Stock Purchase Plan (the “2016 ESPP”). The 2016 ESPP became effective on March 17, 2016. The maximum number of shares of common stock that may be issued under the 2016 ESPP was initially 40,000 shares and automatically increases on January 1 of each year, ending on and including January 1, 2026, by 1.0% of the total number of shares of common stock outstanding on December 31 of the preceding calendar year; provided, however, the Company’s Board of Directors may act prior to the first day of any calendar year to provide that there will be no January 1 increase in the share reserve for such calendar year or that the increase in the share reserve for such calendar year will be a lesser number of shares of common stock. As of March 31, 2026, there were 1,806,922 shares of common stock available for issuance under the 2016 ESPP.
The 2016 ESPP permits participants to purchase shares of the Company’s common stock through payroll deductions of up to 15% of their earnings. Unless otherwise determined by the administrator, the purchase price of the shares will be 85% of the lower of the fair market value of common stock on the first day of an offering or on the date of purchase. Participants may end their participation at any time. The Company initiated its first 2016 ESPP offering period on August 1, 2019. On January 31, 2026, there were 10,125 shares purchased in connection with the offering period. The 2016 ESPP is considered compensatory for financial reporting purposes.
15. |
Fair Value Measurements |
The following table represents the fair value hierarchy of the Company’s financial assets and liabilities measured at fair value on a recurring basis at March 31, 2026 and December 31, 2025 (in thousands):
|
|
March 31, 2026 |
|
||||||||||
Asset Class |
|
Total |
|
Level 1 |
|
Level 2 |
|
Level 3 |
|
||||
Cash and Cash Equivalents⁽¹⁾ |
|
|
|
|
|
|
|
|
|
|
|
|
|
Money market funds |
|
$ |
21,818 |
|
|
21,818 |
|
|
— |
|
|
— |
|
Short Term Investments |
|
|
|
|
|
|
|
|
|
|
|
|
|
Commercial paper (>3 months) |
|
$ |
1,679 |
|
|
— |
|
|
1,679 |
|
|
— |
|
Corporate debt securities |
|
|
12,483 |
|
|
— |
|
|
12,483 |
|
|
— |
|
Government and agency securities (>3 months) |
|
|
20,547 |
|
|
20,547 |
|
|
— |
|
|
— |
|
|
|
December 31, 2025 |
|
||||||||||
Asset Class |
|
Total |
|
Level 1 |
|
Level 2 |
|
Level 3 |
|
||||
Cash and Cash Equivalents⁽¹⁾ |
|
|
|
|
|
|
|
|
|
|
|
|
|
Money market funds |
|
$ |
33,624 |
|
|
33,624 |
|
|
— |
|
|
— |
|
Short Term Investments |
|
|
|
|
|
|
|
|
|
|
|
|
|
Commercial paper (>3 months) |
|
$ |
6,399 |
|
$ |
— |
|
|
6,399 |
|
|
— |
|
Corporate debt securities |
|
|
12,470 |
|
|
— |
|
|
12,470 |
|
|
— |
|
Government and agency securities (>3 months) |
|
|
34,927 |
|
|
34,927 |
|
|
— |
|
|
— |
|
| (1) | Classified as cash and cash equivalents due to their short-term maturity. |
16. |
Income Taxes |
The Company has not recorded any tax provision or benefit for the three months ended March 31, 2026 or 2025. The Company has provided a valuation allowance for the full amount of its net deferred tax assets since realization of any future benefit from deductible temporary differences, NOL carryforwards and research and development credits are not more-likely-than-not to be realized at March 31, 2026 and December 31, 2025.
23
17.Related Party Transactions
PHC has a noncontrolling ownership interest in the Company. In addition, PHC previously appointed two members on the Company’s board of directors (which appointment was terminated on January 1, 2026). The Company previously entered into a financing agreement with PHC on August 9, 2020. Ascensia is a related party through the ownership interests of its parent company, PHC.
Revenue from Ascensia during the three months ended March 31, 2026 and 2025 was $2.4 million and $4.4 million, respectively. Ascensia earned commissions of $0.2 million on sales made through our consignment channel during the three months ended March 31, 2025. No such commissions were incurred during the three months ended March 31, 2026 following the transition of U.S. commercialization activities to the Company.
The amount due from Ascensia as of March 31, 2026 and December 31, 2025 was $4.1 million and $5.3 million, respectively. The amount due to Ascensia as of March 31, 2026 and December 31, 2025 was $8.0 million and $5.2 million, respectively.
As discussed in Note 4, on September 3, 2025 the Company and Ascensia signed a memorandum of understanding (“MOU”) related to the transition of commercial operations for Eversense from Ascensia back to the Company. On December 31, 2025, the parties executed a Master Asset Purchase Agreement, pursuant to which the Company acquired certain U.S. commercial assets and assumed certain related liabilities, with the initial closing on January 1, 2026. In connection with the Master Asset Purchase Agreement, the parties entered into an A&R Commercialization Agreement, which terminated Ascensia’s rights to market Eversense products in the United States and modified Ascensia’s commercialization rights in Europe. The parties are cooperating during a defined transition period to ensure continuity of supply, customer support, and patient access. In connection with this transition, the Company hired certain sales and support personnel previously engaged by the counterparty.
The Company paid total consideration of approximately $1.1 million in connection with the closing of the U.S. asset acquisition (the “U.S. Closing”), prior to customary post-closing adjustments. The acquired assets primarily consisted of returned inventory, a right-of-use asset related to vehicle fleet leases, prepaid marketing expenses, and reimbursement of certain employee-related transition costs associated with personnel hired by the Company. A portion of the consideration related to inventory previously recognized as an estimated return as of December 31, 2025. The Company determined that the U.S. Closing represented an asset acquisition.
As contemplated by the Master Asset Purchase Agreement, on March 12, 2026, the parties entered into separate local asset purchase agreements (the “Local Purchase Agreements”) covering Italy, Germany, Spain and Sweden (the “European Territories”), pursuant to which the Company agreed to acquire certain additional commercial assets (the "European Purchased Assets") and assume certain related liabilities (the “European Assumed Liabilities” and together with the European Purchased Assets, the “European Asset Purchases”) in those territories. The closings of these transactions (the “European Closings”) are subject to customary conditions, including regulatory clearances, consents or non-objection with respect to the transfer of tender contracts and the completion of certain required labor and employment processes, and are expected to occur on or before June 30, 2026.
In connection with the Local Purchase Agreements, the parties also entered into a Transition Services Agreement (the “Transition Services Agreement”) under which Ascensia will provide certain operational and administrative support services in the European Territories during the transition period, including support in the areas of logistics and ordering, payment and collections, claims processing, IT and systems migration, personnel support, finance and operations support, regulatory compliance, and other agreed services, for which the Company will pay certain costs and service fees. The Company incurred approximately $3.2 million of costs under the Transition Services Agreement during the three months ended March 31, 2026, which were primarily recorded in selling, general and administrative expenses.
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18.Segment Information
The Company views its operations and manages its business in one operating segment, which also represents one reportable segment which derives its revenues from diabetes products and services. Operating segments are defined as components of an enterprise about which separate discrete information is available for evaluation by the chief operating decision maker (“CODM”), or decision-making group, in deciding how to allocate resources and in assessing performance. The Company’s CODM, its Chief Executive Officer, manages the Company’s operations on a consolidated basis for the purpose of allocating resources.
The CODM assesses performance for the segment based on net loss, which is reported in the consolidated statements of operations and comprehensive loss and uses the financial information in deciding on how to invest into the Company. The measure of segment assets is reported on the balance sheets as total assets.
The table below summarizes the significant expense categories regularly reviewed by the CODM for the three months ended March 31, 2026 and 2025:
|
|
Three Months Ended |
||||
|
|
March 31, |
||||
|
|
2026 |
|
2025 |
||
Total revenue |
|
$ |
11,711 |
|
$ |
6,257 |
Less: |
|
|
|
|
|
|
Cost of sales |
|
|
4,771 |
|
|
4,752 |
Sales and marketing expenses |
|
|
19,730 |
|
|
1,743 |
Research and development expenses |
|
|
8,611 |
|
|
7,299 |
General and administrative expenses |
|
|
10,445 |
|
|
5,951 |
Other Segment Items(1) |
|
|
487 |
|
|
771 |
Net Loss |
|
$ |
(32,333) |
|
$ |
(14,259) |
| (1) | Other segment items include interest income, interest expense, and other expense as presented in the Company’s consolidated statements of operations and comprehensive loss. |
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19.Subsequent Events
The Company has evaluated all subsequent events through the filing date of this Form 10-Q with the SEC, to ensure that this filing includes appropriate disclosure of events both recognized in the financial statements as of March 31, 2026, and events which occurred subsequently but were not recognized in the financial statements. Except as described below there were no other subsequent events which required recognition, adjustment to or disclosure in the financial statements.
Underwritten Public Offering
On April 30, 2026, the Company entered into an underwriting agreement (the "April 2026 Underwriting Agreement") with TD Securities (USA) LLC and Barclays Capital Inc., as representatives of the several underwriters named therein, pursuant to which the Company agreed to issue and sell an aggregate of 8,000,000 shares of Common Stock and 8,000,000 pre-funded warrants, each representing the right to purchase one share of Common Stock at an exercise price of $0.001 per share (the "May 2026 Pre-Funded Warrants"), at a price to the public of $5.00 per share (or $4.999 per May 2026 Pre-Funded Warrant) (the “May 2026 Offering”). Under the terms of the April 2026 Underwriting Agreement, the Company also granted the underwriters an option, exercisable for 30 days, to purchase up to an additional 2,400,000 shares of Common Stock. The May 2026 Offering closed on May 4, 2026, and the underwriters exercised in full their option to purchase 2,400,000 additional shares of Common Stock. In the aggregate, the Company sold 10,400,000 shares of Common Stock and 8,000,000 May 2026 Pre-Funded Warrants, with aggregate gross proceeds to the Company of approximately $92.0 million, before deducting underwriting discounts and commissions and offering expenses payable by the Company. The net proceeds to the Company were approximately $86.0 million, after deducting underwriting discounts and commissions and estimated offering expenses payable by the Company.
Second Amendment to Loan and Security Agreement
On May 1, 2026, the Company entered into a Second Amendment to Loan and Security Agreement (the “Second Amendment”) with the Lenders and Hercules, which further amended the Amended Loan and Security Agreement. Pursuant to the Second Amendment, the Lenders agreed to make available to the Company up to $140.0 million in senior secured term loans, consisting of (i) the initial term loan of $35.0 million, which was previously funded, (ii) a term loan of $10.0 million (the “2026 Tranche 2 Loan”) to be funded at the closing of the Second Amendment, (iii) four additional tranches of term loans in the amounts of up to $10.0 million (the “2026 Tranche 3A Loan”), $10.0 million (the “2026 Tranche 3B Loan”), $15.0 million (the “2026 Tranche 4 Loan”) and an uncommitted $60.0 million (the “2026 Tranche 5 Loan”), respectively, which will become available to the Company upon the Company's satisfaction of certain terms and conditions set forth in the Amended Loan Agreement. The loans under the Amended Loan Agreement continue to mature on September 3, 2029. The Second Amendment closed on May 6, 2026 (the “Amendment Closing Date”), and both the 2026 Tranche 2 Loan and 2026 Tranche 3A Loan were funded at closing for total proceeds of $20.0 million.
The loans under the Amended Loan Agreement, as modified by the Second Amendment, bear interest at an annual rate equal to the greater of (i) the prime rate as reported in The Wall Street Journal plus 2.40% and (ii) 9.90%. Borrowings are repayable in monthly interest-only payments through (a) October 1, 2028 and (b) if the Company satisfies the 2025 Tranche 3B Milestone (as defined in the Amended Loan Agreement), the Maturity Date. After the interest-only payment period, borrowings are repayable in equal monthly payments of principal and accrued interest until the Maturity Date. At the Company's option, the Company may prepay all or any portion of the outstanding borrowings, subject to a prepayment fee equal to (a) 3.0% of the principal amount being prepaid if the prepayment occurs within one year of the Amendment Closing Date, (b) 2.0% of the principal amount being prepaid if the prepayment occurs during the second year following the Amendment Closing Date, and (c) 1.00% of the principal amount being prepaid if the prepayment occurs more than two years after the Amendment Closing Date and prior to the Maturity Date. In addition, a $100,000 facility fee and a $100,000 amendment fee were payable on the Amendment Closing Date and the Company will pay additional facility fees in the amount of 0.50% of any drawn 2026 Tranche 3B Loan, or in the amount of 1.00% of any drawn 2026 Tranche 4 Loan or 2026 Tranche 5 Loan.
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ITEM 2: MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
Certain statements contained in this Quarterly Report on Form 10-Q may constitute forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. The words or phrases “would be,” “will allow,” “intends to,” “will likely result,” “are expected to,” “will continue,” “is anticipated,” “estimate,” “plan,” “project,” “expect,” or similar expressions, or the negative of such words or phrases, are intended to identify “forward-looking statements.” We have based these forward-looking statements on our current expectations and projections about future events. Because such statements include risks, uncertainties, and assumptions, actual results may differ materially from those expressed or implied by such forward-looking statements. Factors that could cause or contribute to these differences include those described below and elsewhere in this Quarterly Report on Form 10-Q, and in our Annual Report on Form 10-K, particularly in Part I – Item 1A, “Risk Factors,” and our other filings with the Securities and Exchange Commission. Statements made herein are as of the date of the filing of this Quarterly Report on Form 10-Q with the Securities and Exchange Commission and should not be relied upon as of any subsequent date. Unless otherwise required by applicable law, we do not undertake, and we specifically disclaim, any obligation to update any forward-looking statements to reflect occurrences, developments, unanticipated events or circumstances after the date of such statement.
The following discussion and analysis of our financial condition and results of operations should be read in conjunction with our unaudited financial statements and related notes that appear in Item 1 of this Quarterly Report on Form 10-Q and with our audited financial statements and related notes for the year ended December 31, 2025, which are included in our Annual Report on Form 10-K filed with the Securities and Exchange Commission on March 2, 2026. Unless otherwise indicated or the context otherwise requires, all references in this “Management’s Discussion and Analysis of Financial Condition and Results of Operations” section to the “Company,” “we,” “our,” “ours,” “us” or similar terms refer to Senseonics Holdings, Inc. and its consolidated subsidiaries and affiliated entities, as appropriate, including its consolidated VIEs.
Unless otherwise indicated, all information in this Quarterly Report on Form 10-Q gives effect to a 1-for-20 reverse stock split of our common stock that became effective on October 17, 2025 (the “Reverse Stock Split”), and all references to historical share and per share amounts give effect to the Reverse Stock Split.
Overview
We are a medical technology company focused on the design, development and commercialization of glucose monitoring products designed to transform lives in the global diabetes community with differentiated, long-term implantable glucose management technology. Our implantable CGM systems, including the Eversense E3 system (“Eversense E3”) and the Eversense 365 system (“Eversense 365” and, together with Eversense E3, “Eversense” or the “Eversense Systems”), are designed to continually and accurately measure glucose levels in people with diabetes via an under-the-skin sensor, a removable and rechargeable smart transmitter, and a convenient app for real-time diabetes monitoring and management for a period of up to six months in the case of Eversense E3 and up to twelve months in the case of Eversense 365, as compared to seven to 15 days for non-implantable CGM systems. As described in more detail below, in August 2020, we entered into a collaboration and commercialization agreement (“Existing Commercialization Agreement”), with Ascensia Diabetes Care Holdings AG (“Ascensia”) pursuant to which we granted Ascensia the exclusive right to distribute Eversense worldwide, with certain initial exceptions. In February 2022, Eversense E3, a 180 day CGM system, was approved by the FDA and Ascensia began commercializing Eversense E3 in the United States in the second quarter of 2022. In June 2022, we affixed the CE Mark to the extended life Eversense E3 system and Ascensia began commercialization in select markets in Europe during the third quarter of 2022. In September 2024, Eversense 365, a 365-day extended life CGM system, was approved by the FDA and Ascensia began commercializing Eversense 365 in the United States in the fourth quarter of 2024. In January 2026, we took over full commercial responsibility for Eversense 365 in the United States and began marketing and distributing the product with our own sales force. In January 2026, we also obtained CE Mark approval for Eversense 365 and are currently in the process of launching Eversense 365 in Italy, Germany, Spain and Sweden (the “European Territories”).
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On September 3, 2025 the Company and Ascensia signed a memorandum of understanding (“MOU”) related to the transfer of commercial operations relating to Eversense from Ascensia back to the Company. On December 31, 2025, the parties entered into the Master Asset Purchase Agreement formalizing this transfer and subsequently entered into A&R Commercialization Agreement, which terminated Ascensia’s right to market Eversense products in the U.S. and rendered Ascensia’s right to market Eversense products in Italy, Germany, Spain and Sweden (the “European Territories”) non-exclusive. Pursuant to the A&R Commercialization Agreement, effective January 1, 2026, we are entitled to 100% of the revenues derived from the sale of Eversense products in the European Territories. As contemplated by the Master Asset Purchase Agreement, on March 12, 2026 we entered into local asset purchase agreements to facilitate the transition of Ascensia’s commercialization activities in the European Territories and we expect the closings of these transactions to occur on or before June 30, 2026, subject to customary regulatory and operational conditions.
Our net revenues are derived from sales of the Eversense CGM system which includes the Eversense Sensor Pack containing the sensor, insertion tool, and adhesive patches, the Eversense Smart Transmitter Pack containing the transmitter and charger and in some cases the procedure revenue associated with insertions and removals.
We primarily sell directly to our network of distributors and strategic fulfillment partners, who provide the Eversense system to healthcare providers and patients through a prescribed request and invoice insurance payors for reimbursement. In addition, we sell our product through a consignment model through arrangements with our network of healthcare professionals. Sales of the Eversense system are widely dependent on the ability of patients to obtain coverage and adequate reimbursement from third-party payors or government agencies. We leverage and target regions where we have coverage decisions for patient device use and provider insertion and removal procedure payment. We have reached approximately 300 million covered lives in the United States through positive insurance payor coverage decisions. In June 2023, we received positive payor coverage decision from UnitedHealthcare, the largest healthcare insurance company in the United States that effective July 1, 2023, Eversense E3 would be covered. On August 3, 2020, the Center for Medicare and Medicaid Services (“CMS”) released its Calendar Year 2021 Medicare Physician Fee Schedule Proposed Rule that announces proposed policy changes for Medicare payments, including the proposed establishment of national payment amounts for the three CPT© Category III codes describing the insertion (CPT 0446T), removal (0447T), and removal and insertion (0048T) of an implantable interstitial glucose sensor, which describes our Eversense Systems, as a medical benefit, rather than as part of the Durable Medical Equipment channel that includes other CGMs. In December 2021, CMS released its Calendar Year 2022 Medicare Physician Fee Schedule that updated bundled payments for the device cost and procedure fees. In November 2022, CMS released its Calendar Year 2023 Medicare Physician Fee Schedule Proposed Rule that updates the payment amounts for the three CPT© III codes to account for the longer 6-month sensor. In February 2024, we announced that Medicare coverage was expanded for Eversense E3 to include all people with diabetes using insulin and non-insulin users who have a history of problematic hypoglycemia providing access to millions of Medicare patients. In April 2025, CMS updated the payment amounts in the Physician Fee Schedule to account for the longer duration Eversense 365 for all eligible Medicare beneficiaries. The Physician Fee Schedule was updated with similar pricing for 2026. We have been working with payors that previously supported Eversense to transition their policies to Eversense 365 and the majority of these eligible payors have now completed that transition.
In February 2020, we announced that the FDA approved a subgroup of PROMISE trial participants to continue for a total of 365 days to gather feasibility data on the safety and accuracy of a 365-day sensor. This sub-set of 30 participants was left undisturbed for 365 days with the goal of measuring accuracy and longevity over the full 365 days. Information gathered from this sub-set and additional development efforts provided us the confidence to start the ENHANCE pivotal study of Eversense 365. The ENHANCE pivotal study of Eversense 365 completed enrollment, the last patient of the adult cohort completed the study, and we completed our analysis of the data. Based on this analysis, we determined to advance to the next generation sensor platform as the underlying technology used in the 365-day and future products. In May 2024, this data supported an FDA 510(k) submission for a new product with a 365-day duration and once per week calibration. The 510(k) submission was approved by the FDA on September 17, 2024 and Eversense 365 was cleared for sale in the United States.
We continue to expand commercialization of the Eversense brand and are focused on driving awareness of our CGM system amongst people with diabetes and their healthcare providers. Effective January 1, 2026, U.S.
28
commercialization activities were returned to the Company and in Europe, Ascensia continues to sell and market the Eversense product to support the orderly transition of the business to Senseonics anticipated in the second quarter of 2026. In both the United States and our overseas markets we will commercialize the products with direct sales forces and distribution systems that market and promote our various Eversense Systems and future generation products, including our Gemini and Freedom product variations. The Gemini product will allow for a 2-in-1 glucose monitoring system combining the functionality of CGM and flash glucose monitoring, in an implantable sensor with battery that may be utilized with a smart transmitter to get continuous glucose readings and alerts, or be utilized through a swipe over the sensor with a smart phone to get on-demand glucose reading without a smart transmitter. Our Freedom product variation is being designed to include Bluetooth in the sensor, eliminating the on-body component.
United States Development and Commercialization of Eversense
In 2016, we completed our PRECISE II pivotal clinical trial in the United States. This trial, which was fully enrolled with 90 subjects, was conducted at eight sites in the United States. In the trial, we measured the accuracy of the Eversense 90 system (“Eversense 90”) measurements through 90 days after insertion. We also assessed safety through 90 days after insertion or through sensor removal. In the trial, we observed a mean absolute relative difference (“MARD”), of 8.5% utilizing two calibration points for Eversense 90 across the 40-400 mg/dL range when compared to YSI blood reference values during the 90-day continuous wear period. Based on the data from this trial, in October 2016 we submitted a pre-market approval (“PMA”) application to the FDA to market Eversense 90 in the United States for 90-day use. In June 2018, we received PMA approval from the FDA for the Eversense 90 system. In July 2018, we began distributing the 90-day Eversense 90 system directly in the United States through our own direct sales and marketing organization. We have received Category III CPT codes for the insertion and removal of the Eversense 90 sensor.
In December 2018, we initiated the PROMISE pivotal clinical trial to evaluate the safety and accuracy of Eversense 90 for a period of up to six months in the United States and on September 30, 2019, we completed enrollment of the PROMISE trial. In the trial, we observed performance matching that of the then current Eversense 90 available in the United States, with a MARD of 8.5%. This result was achieved with reduced calibration, down to one per day, while also doubling the sensor life to six months. Following the results of the PROMISE trial, on September 30, 2020, a PMA supplement application to extend the wearable life of Eversense 90 to six months was submitted to the FDA. In February 2022, the extended life Eversense E3 was approved by the FDA.
On February 26, 2020, we announced that the FDA approved a subgroup of PROMISE trial participants to continue for a total of 365 days to gather feasibility data on the safety and accuracy of a 365-day sensor. This sub-set of 30 participants was left undisturbed for 365 days with the goal of measuring accuracy and longevity over the full 365 days. Information gathered from this sub-set and additional development efforts provided us with the confidence to start the Pivotal study for Eversense 365.
In April 2020, we announced that we received an extension to our CE Certificate of Conformity in the EEA such that the Eversense XL is no longer contraindicated for MRI, which means the sensor does not need to be removed from under the skin during MRI scanning. We had previously obtained this indication for Eversense 90 in the United States in 2019. This MRI approval is a first for the CGM category, as all other sensors are required to be removed during an MRI scan.
On August 9, 2020, we entered into the Commercialization Agreement pursuant to which we granted Ascensia the exclusive right to distribute Eversense 90 and Eversense E3 worldwide, with certain initial exceptions. Pursuant to the Commercialization Agreement, in the United States, Ascensia began providing sales support for the Eversense 90 product on October 1, 2020 and Ascensia ramped up sales activities and assumed commercial responsibilities for Eversense 90 during the second quarter of 2021.
On September 3, 2025, the Company and Ascensia signed the MOU related to the transfer of commercial operations relating to Eversense from Ascensia back to the Company, including the proposed termination, orderly unwinding of, and smooth transition of the commercial relationship between the Company and Ascensia. On December 31, 2025, the Company and Ascensia entered into the Master Asset Purchase Agreement, pursuant to which, among other things, the Company agreed to acquire Ascensia’s right, title and interest in and to certain assets related to the marketing, selling and distribution of Eversense in the United States (such assets, the “U.S.
29
Purchased Assets”).
Pursuant to the terms of the Master Asset Purchase Agreement, the Company agreed to assume certain liabilities and obligations associated with the U.S. Purchased Assets (the “U.S. Assumed Liabilities” and together with the U.S. Purchased Assets, the “U.S. Asset Purchase”), including, but not limited to, certain liabilities under the contracts transferred to the Company under the Master Asset Purchase Agreement, liabilities arising out of the use or ownership of the transferred assets after the closing, and liabilities and obligations arising from certain employees who were offered employment with Senseonics Inc. pursuant to new employment letter agreements. The U.S. Asset Purchase closed on January 1, 2026 (the “U.S. Closing”).
In connection with the execution of the Master Asset Purchase Agreement, the Company and Ascensia also entered into the A&R Commercialization Agreement on December 31, 2025, which amended and restated the Existing Commercialization Agreement. The A&R Commercialization Agreement terminated Ascensia’s right to market Eversense products in the U.S. Following the U.S. Closing, Ascensia has no further rights to revenues from the sale of Eversense products in the U.S.
In February 2022, we received approval from the FDA for Eversense E3. The approval for our third-generation sensor, with proprietary sacrificial boronic acid (“SBA”) technology doubles the sensor life to six months with MARD of 8.5%. Ascensia began commercializing Eversense E3 in the United States during the second quarter of 2022.
The ENHANCE clinical study was initiated as a pivotal study with the purpose of gathering additional clinical data to support an integrated continuous glucose monitoring (“iCGM”) submission for Eversense E3 using the SBA technology. In March 2022, we extended the ongoing ENHANCE clinical study to evaluate the safety and accuracy of Eversense 365 for a period of up to one year in the United States. In September 2022, we completed enrollment of the ENHANCE study and the last patient of the adult cohort completed the study in the third quarter of 2023. In November 2022, we submitted and in the first quarter of 2023 we received approval of an investigational device exemption (“IDE”) for the enrollment of a pediatric cohort in the ENHANCE study. In 2023 the data gathered in the ENHANCE study supported the iCGM submission and in April 2024, Eversense 365 was authorized to be marketed as an iCGM through the FDA’s De Novo pathway, by establishing the special controls that will serve as a predicate device for 510(k) submissions in the future. Based on the analysis of the ENHANCE Pivotal study data, the decision was made to advance to the next generation sensor platform as the underlying technology used in the 365-day and future products. In May 2024, this data supported an FDA 510(k) submission for a new product with a 365-day duration and once per week calibration. The 510(k) submission was approved by the FDA on September 17, 2024 and Eversense 365 product was cleared for sale in the United States. Ascensia began commercializing Eversense 365 in the United States during the fourth quarter of 2024.
In an effort to accelerate commercialization efforts and address challenges to Eversense adoption, in April 2024 and July 2024, we established new legal entities, Eon Care Services, LLC and Eon Management Services, LLC, which were formed as wholly owned subsidiaries of Senseonics, Incorporated. In November 2024, Eon Management Services, LLC entered into management services agreements (the “Administrative Agreement”) for an initial fixed term of 10 years with the Eon Care PCs, which were created to support patient access to the Eversense Systems by contracting nurse practitioners and other healthcare professionals to perform Eversense insertion procedures and other clinical activities. On April 1, 2026, Eon Management Services, LLC entered into an additional management services agreement with an additional professional corporation with an initial fixed term of 10 years. The Eon Care PCs are consolidated as VIEs.
The wholly owned entities and Eon Care PCs (collectively, “Eon Care”) were established to support patient access to the Eversense systems by providing convenient Eversense insertion and training services. We fully completed the transition of our network of inserters from the Nurse Practitioner Group to Eon Care in the second quarter of 2025, and we experienced an increase in the number of insertions since then. Once we build out and establish the Eon Care network, we expect established CPT codes associated with Eversense insertions to enable a self-sustaining economic model for this initiative in the future.
30
We have also sought to complement commercialization efforts by establishing a consignment program, whereby we sell the Eversense system and related components and supplies through a network of healthcare professionals, and supporting certain commercial programs such as direct to consumer (“DTC”) spending, certain key account activities, and market access support. We are determined to increase investment in supporting DTC spending, which we believe correlates with higher awareness and adoption of Eversense. Although the rate of Eversense adoption and lead generation has increased following these initiatives, as well as the regulatory approval of Eversense 365, we continue to work on ways to accelerate commercialization and adoption of our product.
In July 2024, we began first-in-human testing for the Gemini product. The next-generation Gemini product utilizes a fully implantable self-powering system that includes a flash glucose monitor with no on-body component for people with type 2 diabetes and traditional CGM with an on-body component for people with type 1 diabetes. The Gemini product is built on the 365-day sensor platform and the clinical and regulatory work will be focused on demonstrating the battery integration and functionality rather than the sensor life. Data gathered from this first-in-human testing was utilized for an IDE submission that was approved by the FDA in December 2025 which allowed us to begin enrolling patients in the Gemini pivotal study.
European Commercialization of Eversense
In September 2017, we affixed the CE Mark for Eversense XL which permits the product to be sold freely in any part of the EEA. Eversense XL is indicated for a sensor life of up to 180 days. Eversense XL began commercialization in Europe in the fourth quarter of 2017. All such commercialization and marketing activities remain subject to applicable government approvals.
In June 2022, we affixed the CE Mark to Eversense E3, and Ascensia began commercialization in European markets during the second half of 2022.
In February 2025, we submitted an application for the conformity assessment of Eversense 365 to our Notified Body for certification. The submission was prepared in compliance with the EU medical device regulation. In January 2026, the Company obtained CE Mark approval for Eversense 365 and are currently in the process of launching Eversense 365 in the European Territories.
The A&R Commercialization Agreement rendered Ascensia’s right to market Eversense products in the European Territories non-exclusive. Ascensia agreed to continue to sell and market the Eversense product in Europe to support the orderly transition of the business pending the closing of the European Asset Purchases and to allow Senseonics to transfer its local tender contracts. These rights and obligations apply from January 1, 2026 until the later of (i) January 1, 2027, (ii) the transfer of all local tender contracts, or (iii) the wind down of certain other commercial activities. Pursuant to the A&R Commercialization Agreement, effective January 1, 2026, the Company is entitled to 100% of the revenues derived from the sale of Eversense products in the European Territories. Senseonics will pay for certain transition services, and certain other costs, to maintain and achieve the orderly transition of the commercial operations in the European Territories. The Company and Ascensia executed separate local asset purchase agreements in the European Territories on March 12, 2026, in connection with the European Asset Purchases.
Financial Overview
A significant portion of our product revenue has historically been generated from sales of the Eversense system and related components and supplies to Ascensia, through the Commercialization Agreement, who then resells the products to health care providers and patients. Effective January 1, 2026, in connection with the transition of U.S. commercialization activities to the Company, we began generating a greater portion of our product revenue through direct sales to strategic fulfillment partners and through our consignment network in the United States, while Ascensia continues to support commercialization activities outside the United States during a defined transition period.
Revenue from product sales to Ascensia is recognized at a point in time when Ascensia obtains control of our product based upon the delivery terms as defined in the contract at an amount that reflects the consideration which we expect to receive in exchange for the product. Our contract with Ascensia contains performance obligations, mostly for the supply of goods, and are typically satisfied upon transfer of control of the product and does not include the right to return unless there is a product issue, in which case we may provide replacement product.
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Product conformity guarantees do not create additional performance obligations and are accounted for as warranty obligations in accordance with guarantee and loss contingency accounting guidance.
The consideration we expect to receive includes estimates of variable consideration for which reserves are established that is primarily the result of variable consideration such as patient assistance program rebates, prompt-pay discounts, tier-volume price discounts and for the Commercialization Agreement, revenue share. Variable consideration, such as rebates and prompt-pay incentives, are treated as a reduction in revenue and variable considerations, such as revenue share, is treated as an addition in revenue when the product sale is recognized. The amount of variable consideration that is included in the transaction price may be constrained and is included in revenue only to the extent that it is probable that a significant reversal in the amount of the cumulative revenue recognized will not occur in a future period, when the uncertainty associated with the variable consideration is subsequently resolved. Estimating variable consideration and the related constraint requires the use of significant management judgment. Depending on the variable consideration, we develop estimates for the expected value based on the terms of the agreements, historical data, geographic mix, reimbursement rates, and market conditions. Variances in the consideration recognized is partially mitigated by minimum price provisions for certain purchases under the contract.
Under the consignment model, small quantities of inventory are held at healthcare provider locations to ensure availability when a patient is identified. No revenue is recognized upon delivery of our products to the healthcare provider locations, as we retain the ability to control the inventory. Rather, revenue is recognized when the product is consumed by a patient.
Contract assets consist of unbilled receivables from customers and are recorded at net realizable value and relate to the timing of billings and revenue share variable consideration from the Commercialization Agreement.
Concentration of Revenue and Customers
A significant portion of the Company’s revenue has historically been derived from one customer, Ascensia. For the three months ended March 31, 2026 and 2025, sales to Ascensia accounted for 20% and 71% of total revenue, respectively.
A portion of the Company’s revenue is earned under consignment arrangements with healthcare providers. For the three months ended March 31, 2026 and 2025, sales under consignment arrangements accounted for 37.3% and 19.6% of total revenue, respectively. During 2025, Ascensia earned commission on sales made through these consignment arrangements for the support provided by their sales reps and commercial organization. Revenues for these corresponding periods represent sales of sensors, transmitters and miscellaneous Eversense System components.
Termination and Modification of Commercialization Arrangements
On September 3, 2025 the Company and Ascensia signed a memorandum of understanding related to the transfer of commercial operations relating to Eversense from Ascensia back to the Company, including the proposed termination, orderly unwinding of, and smooth transition of the commercial relationship between the Company and Ascensia. On December 31, 2025, the parties entered into the Master Asset Purchase Agreement and the A&R Commercialization Agreement, pursuant to which commercial activities in the United States transitioned back to the Company effective January 1, 2026 and the commercialization rights in certain European Territories were modified to be non-exclusive. The parties continue to cooperate through the transition period to ensure continuity of supply, customer support, and patient access. Following the execution of the A&R Commercialization Agreement, the Company will no longer recognize revenue associated with U.S. product sales to Ascensia under the distribution arrangement. As a result, our revenues and results of operations will not be directly comparable to our historical revenues and results of operations for periods in which the Commercialization Agreement was in place.
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Revenue by Geographic Region
The following table sets forth net revenue derived from our two primary geographical markets, the United States and outside of the United States, based on the geographic location to which we deliver the product, for the three months ended March 31, 2026 and 2025:
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Three Months Ended |
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|
March 31, 2026 |
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|
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% |
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|
(Dollars in thousands) |
|
Amount |
|
of Total |
|
|
Revenue, net: |
|
|
|
|
|
|
United States |
|
$ |
9,330 |
|
79.7 |
% |
Outside of the United States |
|
|
2,381 |
|
20.3 |
|
Total |
|
$ |
11,711 |
|
100.0 |
% |
|
|
|
|
|
|
|
|
|
Three Months Ended |
|
|||
|
|
March 31, 2025 |
|
|||
|
|
|
|
% |
|
|
(Dollars in thousands) |
|
Amount |
|
of Total |
|
|
Revenue, net: |
|
|
|
|
|
|
United States |
|
$ |
4,495 |
|
71.8 |
% |
Outside of the United States |
|
|
1,762 |
|
28.2 |
|
Total |
|
$ |
6,257 |
|
100.0 |
% |
Results of Operations for the Three Months Ended March 31, 2026 and 2025
|
|
Three Months Ended |
|
|
|
|
||||
|
|
March 31, |
|
Period-to- |
|
|||||
|
|
2026 |
|
2025 |
|
Period Change |
|
|||
|
|
(in thousands) |
|
|
(in thousands) |
|
||||
Revenue, net |
|
$ |
9,341 |
|
$ |
1,810 |
|
$ |
7,531 |
|
Revenue, net - related parties |
|
|
2,370 |
|
|
4,447 |
|
|
(2,077) |
|
Total revenue |
|
|
11,711 |
|
|
6,257 |
|
|
5,454 |
|
Cost of sales |
|
|
4,771 |
|
|
4,752 |
|
|
19 |
|
Gross profit |
|
|
6,940 |
|
|
1,505 |
|
|
5,435 |
|
|
|
|
|
|
|
|
|
|
|
|
Expenses: |
|
|
|
|
|
|
|
|
|
|
Research and development expenses |
|
|
8,611 |
|
|
7,299 |
|
|
1,312 |
|
Selling, general and administrative expenses |
|
|
30,175 |
|
|
7,694 |
|
|
22,481 |
|
Operating loss |
|
|
(31,846) |
|
|
(13,488) |
|
|
(18,358) |
|
Other (expense) income, net: |
|
|
|
|
|
|
|
|
|
|
Interest income |
|
|
742 |
|
|
675 |
|
|
67 |
|
Interest expense |
|
|
(1,192) |
|
|
(1,429) |
|
|
237 |
|
Other expense |
|
|
(37) |
|
|
(17) |
|
|
(20) |
|
Total other income (expense), net |
|
|
(487) |
|
|
(771) |
|
|
284 |
|
Net Loss |
|
$ |
(32,333) |
|
$ |
(14,259) |
|
$ |
(18,074) |
|
Total revenue
Our total revenue increased to $11.7 million for the three months ended March 31, 2026, compared to $6.3 million for the three months ended March 31, 2025, an increase of $5.4 million. This increase was primarily driven by sales growth in the US largely due to growth in the consignment program and 365-day product demand. The increase in total revenue was further driven by the elimination of Ascensia revenue share amounts following the termination of Ascensia's commercialization rights in the United States and the transition of commercialization activities in the European Territories to a non-exclusive arrangement.
33
Cost of sales and gross profit
Our cost of sales remained consistent at $4.8 million for the three months ended March 31, 2026 and the three months ended March 31, 2025. Our gross profit increased to $6.9 million for the three months ended March 31, 2026, compared to $1.5 million for the three months ended March 31, 2025. Gross profit as a percentage of revenue, or gross margin, was 59.3% and 24.1% for the three months ended March 31, 2026, and March 31, 2025, respectively. The improvement in gross margin is largely driven by favorable margins on the 365-day product sales, higher consignment network sales with ASP favorability, the elimination of the Ascensia revenue share and consistent fixed manufacturing costs. In addition, we recognized a one-time benefit of $0.5 million related to a change in estimate of previously accrued E3 product shutdown costs.
Research and development expenses
Research and development expenses were $8.6 million for the three months ended March 31, 2026, compared to $7.3 million for the three months ended March 31, 2025, an increase of $1.3 million. This increase was primarily driven by the ramp up of our Gemini pivotal study driving efforts to eliminate the on-body transmitter component and additional product development projects.
Selling, general and administrative expenses
Selling, general and administrative expenses were $30.2 million for the three months ended March 31, 2026, compared to $7.7 million for the three months ended March 31, 2025, representing an increase of $22.5 million. The increase consisted of $18.0 million higher selling and marketing costs largely driven by re-assuming commercialization activities resulting in a large increase in our headcount and increased marketing spend largely consisting of direct-to-consumer marketing initiatives. Our total general and administrative costs increased by $4.5 million driven by newly assumed operational responsibilities related to the commercial integration, as well as legal, IT and consulting costs associated with the establishment of business operations to support the transition of European commercialization activities to the Company.
Total other income (expense), net
Total other income (expense), net was $(0.5) million for the three months ended March 31, 2026, compared to other expense, net of ($0.8) million for three months ended March 31, 2025, a decrease in other income (expense), net of $0.3 million. The change was primarily due to a $0.2 million decrease in interest expense offset by a $0.1 million increase in interest income.
Liquidity and Capital Resources
Sources of Liquidity
From its founding in 1996 until 2010, the Company has devoted substantially all of its resources to researching various sensor technologies and platforms. Beginning in 2010, the Company narrowed its focus to developing and refining a commercially viable glucose monitoring system. The Company has incurred substantial losses and cumulative negative cash flows from operations since its inception in October 1996 and expects to incur additional losses in the near future. We incurred total net loss of $(69.1) million and $(78.6) million for the years ended December 31, 2025 and 2024, respectively. For the three months ended March 31, 2026, the Company had a net loss of $(32.3) million, and an accumulated deficit of $(1.0) billion. To date, the Company has funded its operations principally through the issuance of preferred stock, common stock, warrants, convertible notes, and debt. As of March 31, 2026, the Company had unrestricted cash, cash equivalents, and marketable securities of $64.3 million.
34
In the recent years, we have taken a number of measures to strengthen our financial position, including but not limited to the following actions:
Equity Offerings
In August 2025, we entered into an at-the-market sales agreement (the “Sales Agreement”) with TD Securities (USA) LLC (“TD Cowen”), under which we may offer and sell, from time to time, at our sole discretion, shares of common stock having an aggregate offering price of up to $100.0 million through TD Cowen as its sales agent in an “at the market” offering. TD Cowen will receive commissions up to 3.0% of the gross proceeds of any common stock sold through TD Cowen under the Sales Agreement. The shares will be offered and sold pursuant to an effective shelf registration statement on Form S-3, which was originally filed with the Securities and Exchange Commission on August 6, 2025. During the twelve months ended December 31, 2025, we received approximately $2.4 million proceeds from the sale of 334,330 shares under the Sales Agreement, after deducting sales commissions and offering expenses. During the three months ended March 31, 2026, the Company received approximately $3.5 million proceeds from the sale of 478,067 shares under the Sales Agreement, after deducting sales commissions and offering expenses. As of March 31, 2026, an aggregate of $93.8 million remained available for issuance under the Sales Agreement.
On April 30, 2026, we entered into an underwriting agreement with TD Cowen and Barclays Capital Inc., as representatives of the several underwriters named therein, for the sale of shares of Common Stock and pre-funded warrants, each representing the right to purchase one share of Common Stock at an exercise price of $.001 per share (the “May 2026 Pre-Funded Warrants”), at a price to the public of $5.00 per share (or $4.999 per May Pre-Funded Warrant) (the “May 2026 Offering”). The May 2026 Offering closed on May 4, 2026, and the underwriters exercised in full their option to purchase 2,400,000 additional shares of Common Stock. In the aggregate, we sold 10,400,000 shares of Common Stock and 8,000,000 May 2026 Pre-Funded Warrants in the May 2026 Offering, generating aggregate gross proceeds of approximately $92.0 million, before deducting underwriting discounts and commissions and offering expenses payable by us. The net proceeds to Senseonics were approximately $86.0 million, after deducting underwriting discounts and commissions and estimated offering expenses. The securities were offered and sold pursuant to an effective shelf registration statement on Form S-3 (File No. 333-289306).
Indebtedness
Amended Loan and Security Agreement
On September 8, 2023, the Company entered into the Loan and Security Agreement with the Lenders and Hercules. The Company and Hercules have amended this agreement on two occasions, most recently on May 1, 2026 (as amended, the “Amended Loan and Security Agreement”). Under the Amended Loan and Security Agreement, the Lenders have agreed to make available to the Company the Term Loan Facility, providing for an aggregate of up to $140.0 million of loans. To date, Hercules and the Lenders have extended term loans to the Company in the aggregate amount of $55.0 million. The Amended Loan and Security Agreement provides for additional potential borrowings in the aggregate amount of up to $85 million, which may be extended in three tranches of up to $10.0 million, up to $15.0 million, and up to $60.0 million, respectively, which will become available to the Company upon the Company’s satisfaction of certain terms and conditions set forth in the Amended Loan and Security Agreement and, in the case of the $60 million tranche, the Lenders’ investment committee approval. The loans under the Amended Loan and Security Agreement mature on September 3, 2029. The Company received proceeds from the Tranche 2 Loan and an additional $10.0 million tranche (the “Tranche 3A Loan”) upon the closing of the Second Amendment to the Loan and Security Agreement (the “Second Amendment”) on May 6, 2026.
Convertible Notes
The 2025 Notes were repaid in full on January 15, 2025. See Note 12 in the accompanying notes to our consolidated financial statements included elsewhere in this 10-Q for further discussion of the 2025 Notes.
35
Funding Requirements and Outlook
Our ability to grow revenues and achieve profitability depends on the successful commercialization and adoption of our Eversense System by diabetes patients and healthcare providers, along with future product development, regulatory approvals, and post-approval requirements. Successful completion of the transfer of commercial operations relating to Eversense from Ascensia back to the Company may provide opportunities to have greater influence on revenue generation and market adoption of Eversense. These activities, including our ongoing focus to grow covered lives through positive insurance payor policy decisions, initiatives to support patient access, and continued development of Eversense 365, will require significant uses of working capital through 2026 and beyond. As of March 31, 2026, the Company had unrestricted cash, cash equivalents and marketable securities of $64.3 million.
In accordance with the FASB Accounting Standards Codification Topic 205-40, Presentation of Financial Statements- Going Concern, management is required to assess the Company’s ability to continue as a going concern through twelve months after issuance of the financial statements. Management previously disclosed conditions and events that raised substantial doubt about our ability to continue as a going concern. In addition, given the Company’s historical reliance upon debt and equity financing, management will continue to evaluate our funding needs against operating performance and strategic initiatives.
As of the first quarter of 2026, based on current operating plans, the subsequent receipt of financing proceeds (as further described under “Sources of Liquidity”), its existing unrestricted cash, cash equivalents, and marketable securities management now believes that the Company has sufficient resources to meet the Company’s anticipated operating needs for the next twelve months from the issuance of the financial statements. Accordingly, management has concluded that the substantial doubt that was raised in the past about the Company’s ability to continue as a going concern has been alleviated.
Cash Flows
The following is a summary of cash flows for each of the periods set forth below (in thousands).
|
|
Three Months Ended |
|
||||||
|
|
March 31, |
|
||||||
|
|
2026 |
|
2025 |
|
||||
Net cash used in operating activities |
|
$ |
(32,025) |
|
$ |
(16,080) |
|
||
Net cash provided by (used in) investing activities |
|
|
17,996 |
|
|
(25,325) |
|
||
Net cash provided by financing activities |
|
|
3,407 |
|
|
6,119 |
|
||
Net decrease in cash, cash equivalents and restricted cash |
|
$ |
(10,622) |
|
$ |
(35,286) |
|
||
Net cash used in operating activities
Net cash used in operating activities was $32.0 million for the three months ended March 31, 2026, and consisted of a net loss of $32.3 million and a net change in operating assets and liabilities of $2.7 million (most notably increases in accounts receivable of $3.0 million, inventory of $1.3 million, and accrued expenses and other liabilities of $3.0 million), partially offset by a $2.3 million increase of stock-based compensation, and a $0.7 million increase related to depreciation/amortization and other non-cash items.
Net cash used in operating activities was $16.1 million for the three months ended March 31, 2025, and consisted of a net loss of $14.3 million and a net change in operating assets and liabilities of $4.8 million (most notably decreases in accrued expenses and other liabilities of $5.7 million and accounts payable of $0.9 million, net of decreases in accounts receivable of $1.7 million and prepaid expenses and other current assets of $1.0 million), partially offset by $1.8 million of stock-based compensation and $1.1 million related to depreciation/amortization and other non-cash items.
36
Net cash provided by (used in) investing activities
Net cash provided by investing activities was $18.0 million for the three months ended March 31, 2026, and consisted of $23.3 million in proceeds from the sale of marketable securities, partially offset by $4.0 million in purchases of marketable securities and $1.1 million related to the acquisition of U.S. commercialization assets from Ascensia.
Net cash used in investing activities was $25.3 million for the three months ended March 31, 2025, and consisted of $24.9 million in purchases of marketable securities and $0.4 million of capital expenditures.
Net cash provided by financing activities
Net cash provided by financing activities was $3.4 million for the three months ended March 31, 2026, and primarily consisted of $3.5 million in proceeds from the issuance of common stock and $0.1 million of proceeds from the exercise of stock options, RSUs, and ESPP issuances, partially offset by $0.2 million of taxes paid related to net share settlement of equity awards.
Net cash provided by financing activities was $6.1 million for the three months ended March 31, 2025, and primarily consisted of $26.5 million in proceeds from the issuance of common stock net offset by $20.4 million used to repay the remaining outstanding 2025 Notes.
ITEM 3: Quantitative and Qualitative Disclosures About Market Risk
Under SEC rules and regulations, because we are considered to be a “smaller reporting company”, we are not required to provide the information required by this item in this Quarterly Report on Form 10-Q.
ITEM 4: Controls and Procedures
Evaluation of Disclosure Controls and Procedures
Our management, with the assistance of our chief executive officer, who is our principal executive officer, and our chief financial officer, who is our principal financial officer, has reviewed and evaluated the effectiveness of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934, as amended) as of March 31, 2026. Management recognizes that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving their objectives and management necessarily applies its judgment in evaluating the cost-benefit relationship of possible controls and procedures. Our disclosure controls and procedures include controls and procedures designed to ensure that information required to be disclosed by us in the periodic reports filed with the SEC is accumulated and communicated to our management, including our principal executive, financial and accounting officers, or persons performing similar functions, as appropriate to allow timely decisions regarding required disclosure. Our disclosure controls and procedures are designed to provide reasonable assurance of achieving such control objectives. Based on the evaluation of our disclosure controls and procedures as of March 31, 2026, our chief executive officer and chief financial officer concluded that, as of such date, our disclosure controls and procedures were effective at the reasonable assurance level.
Changes in Internal Control over Financial Reporting
There were no changes in our internal control over financial reporting identified in connection with the evaluation required by Rule 13a-15(d) and 15d-15(d) of the Exchange Act that occurred during the quarter ended March 31, 2026 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.
37
PART II: OTHER INFORMATION
ITEM 1: Legal Proceedings
From time to time, we are subject to litigation and claims arising in the ordinary course of business. Although the results of litigation and claims cannot be predicted with certainty, we currently believe that the final outcome of these ordinary course matters will not have a material adverse effect on our business. Legal proceedings, including litigation, government investigations and enforcement actions could result in material costs, occupy significant management resources and entail civil and criminal penalties.
In May 2024, the Company received notice and accepted service of a civil complaint that had been filed in the Eastern District of Texas and styled Cellspin Soft, Inc. vs. Senseonics Holdings, Inc., and Ascensia Diabetes Care Holdings AG Case No. 2:24-cv 263. The case was filed by a non-practicing entity alleging patent infringement of three patents. The validity of all three of these patents were challenged in Inter Partes Review proceedings at the U.S. Patent and Trademark Office by another party, TikTok Inc., (the “TikTok IPR”) and on September 30, 2024, the Patent Trial and Appeal Board instituted a review with respect to each of the asserted claims in these three patents. Together with LifeScan, Inc. and Ascensia, on October 30, 2024, we filed a joint motion to join the TikTok IPR as well as our own joint independent, similar Inter Partes Review (the “Senseonics IPR”) petitions challenging these patents. On February 5, 2025, the court issued an order staying the proceedings in the Eastern District of Texas pending resolution of the Inter Partes Reviews. On June 5, 2025, prior to the imminent TikTok IPR final hearings, the Acting Director of the U.S. Patent and Trademark Office ordered a sua sponte review by the Acting Director of whether the TikTok IPR could proceed based on certain novel issues relating to TikTok’s Chinese ownership status. On January 23, 2026, the Director of the U.S. Patent and Trademark Office issued and order stating that, in view of a recent order by the Patent Trial and Appeal Board and TikTok Inc.’s announced Joint Venture (and the referenced ownership attributes thereof), the parties were authorized to file an additional brief addressing whether the evidence Cellspin Soft, Inc. submitted is sufficient to put TikTok Inc.’s real party in interest identification into dispute, and what effect, if any, the announced Joint Venture has on the TikTok IPR proceedings. TikTok, Inc. and Cellspin Soft, Inc. filed additional briefs on February 2, 2026. On March 30, 2026, the Director of the U.S. Patent and Trademark Office issued an order vacating the Board’s decisions granting institution of the TikTok IPR and denied the TikTok IPR petitions. The Director also vacated the Board’s order joining the Senseonics IPR to the TikTok IPR, and ordered the Board to determine whether the Senseonics IPR should be instituted on their own. On April 15, 2026, the Board granted institution of the Senseonics IPR on all three patents involved in the district court litigation. The Board further ordered that a final hearing will be held on June 30, 2026 on the Senseonics IPR. On April 20, 2026, Cellspin requested rehearing of the Board’s April 15, 2026 institution decisions. On April 28, 2026, the Board denied Cellspin’s requests for rehearing. Should any asserted claim in the three patents survive the invalidity challenge in the Senseonics Inter Partes Review proceedings, the Company intends to vigorously defend the lawsuit. The proceedings in the Eastern District of Texas remain stayed pending resolution of the Senseonics IPR.
Except as described above, we are not currently a party to any material legal proceedings, and we are not aware of any pending or threatened legal proceeding against us that we believe could have a material adverse effect on our business, operating results or financial condition.
ITEM 1A: Risk Factors
Our business is subject to risks and events that, if they occur, could adversely affect our financial condition and results of operations and the trading price of our securities. Except as set forth below, there have been no material changes from our risk factors described in “Part I, Item 1A. Risk Factors” of our Annual Report on Form 10-K for the year ended December 31, 2025, as filed with the SEC on March 2, 2026, except for the following:
38
Risks Relating to our Business and our Industry
The consummation of the European Asset Purchases is subject to conditions that may not be satisfied, and delays or failures in completing the European Closings could adversely affect our business, financial condition and results of operations.
On March 12, 2026, we entered into the Local Purchase Agreements with Ascensia, pursuant to which we agreed to acquire certain commercial assets and assume certain related liabilities in Italy, Germany, Spain and Sweden. The closing of each of the European Asset Purchases is subject to the satisfaction or waiver of customary closing conditions, including the obtaining of certain regulatory clearances, consents or non-objection with respect to the transfer of tender contracts and the completion of certain required labor and employment processes. There can be no assurance that these conditions will be satisfied or waived in a timely manner, or at all. Potential delays in consummating the European Closings could result in increased execution costs, diversion of management attention and resources, and prolonged reliance on Ascensia for transition services under the Transition Services Agreement, which could increase our operating expenses. In addition, the assumption of direct commercial responsibility for Eversense in the European Territories involves significant operational risks, including potential disruptions in relationships with employees, patients, prescribers, distributors or regulatory authorities. We will be required to establish or expand local operations, hire or retain qualified personnel, and comply with local regulatory requirements in each of the European Territories. If we are unable to successfully complete the European Asset Purchases or effectively manage the transition of commercial operations, our ability to generate revenue in the European Territories could be materially adversely affected, and we may incur significant costs that could harm our financial condition and results of operations.
Risks Related to our Financial Results and Need for Financing
Future borrowings under the Second Amendment to our Amended Loan and Security Agreement with Hercules Capital, Inc. are subject to conditions that may not be satisfied, and we may not have access to the full amount of the facility.
On May 1, 2026, we entered into the Second Amendment to our Amended Loan and Security Agreement with Hercules (the “Second Amendment”), which increased the total loan potential borrowings under the agreement from $100.0 million to $140.0 million. As of the date of this report, we have drawn an aggregate of $55 million of borrowings under the Hercules facility. However, future borrowings under the agreement are subject to the satisfaction of certain terms and conditions and, with respect to the final $60.0 million, the approval of Hercules’s investment committee. There can be no assurance that such conditions to funding will be satisfied. If we are unable to access the full amount of the facility, we may not have sufficient liquidity to fund our operations and may need to seek additional financing on terms that may be less favorable, or we may not be able to obtain additional financing at all.
Our increased indebtedness under the amended Hercules facility may adversely affect our financial condition, and we may not be able to maintain compliance with the financial covenants contained therein.
As a result of the Second Amendment, we have the potential to incur significantly greater indebtedness under the amended Hercules facility. Increased indebtedness could, among other things, increase our vulnerability to general adverse economic and industry conditions, limit our flexibility in planning for or reacting to changes in our business and the industry in which we operate, and place us at a competitive disadvantage compared to our competitors that have less debt. In addition, we will be required to comply with financial and other covenants in the amended facility and our ability to comply with these covenants will depend on our future operating performance, which is subject to prevailing economic conditions and other factors, many of which are beyond our control. If we fail to comply with these covenants, we could be in default under the facility, which could result in the acceleration of all outstanding indebtedness thereunder and materially adversely affect our financial condition and ability to continue as a going concern.
39
ITEM 2: Unregistered Sales of Equity Securities and Use of Proceeds
Not applicable.
ITEM 3: Defaults Upon Senior Securities
Not applicable.
ITEM 4: Mine Safety Disclosures
Not applicable.
ITEM 5: Other Information
During the fiscal quarter ended March 31, 2026, none of our directors and officers (as defined in Rule 16a-1(f) under the Securities and Exchange Act of 1934, as amended) adopted, modified or terminated the contracts, instructions or written plans for the purchase or sale of the Company’s securities.
40
ITEM 6: Exhibits
The exhibits listed on the Exhibit Index hereto are filed or incorporated by reference (as stated therein) as part of this Quarterly Report on Form 10-Q.
|
||
Exhibit No. |
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Document |
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2.1*# |
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2.2*# |
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2.3*# |
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2.4*# |
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|
|
|
2.5*# |
|
|
|
|
|
3.1 |
|
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|
|
|
3.2 |
|
|
|
|
|
3.3 |
|
|
|
|
|
3.4 |
|
|
3.5 |
|
|
|
|
|
3.6 |
|
|
|
|
|
3.7 |
|
|
|
|
|
3.8 |
|
|
|
|
|
3.9 |
|
|
|
|
|
10.1 |
|
|
10.2*# |
|
|
|
|
|
10.3*# |
|
|
41
31.1* |
|
Certification of Principal Executive Officer under Section 302 of the Sarbanes-Oxley Act. |
|
|
|
31.2* |
|
Certification of Principal Financial Officer under Section 302 of the Sarbanes-Oxley Act. |
|
|
|
32.1** |
|
|
|
|
|
101.INS* |
|
Inline XBRL Instance Document (the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the inline XBRL document) |
|
|
|
101.SCH* |
|
Inline XBRL Taxonomy Extension Schema Document |
|
|
|
101.CAL* |
|
Inline XBRL Taxonomy Extension Calculation Linkbase Document |
|
|
|
101.DEF* |
|
Inline XBRL Taxonomy Extension Definition Linkbase Document |
|
|
|
101.LAB* |
|
Inline XBRL Taxonomy Extension Label Linkbase Document |
|
|
|
101.PRE* |
|
Inline XBRL Taxonomy Extension Presentation Linkbase Document |
|
|
|
104 |
|
Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101) |
* |
Filed herewith. |
** |
These certifications are being furnished solely to accompany this quarterly report pursuant to 18 U.S.C. Section 1350, and are not being filed for purposes of Section 18 of the Exchange Act and are not to be incorporated by reference into any filing of the registrant, whether made before or after the date hereof, regardless of any general incorporation language in such filing. |
# |
Certain portions of this exhibit, indicated by asterisks, have been omitted because they are not material and are the type that the registrant treats as private and confidential. |
42
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
|
SENSEONICS HOLDINGS, INC. |
|
|
|
|
|
|
|
Date: May 7, 2026 |
By: |
/s/Rick Sullivan |
|
|
Rick Sullivan |
|
|
Chief Financial Officer |
|
|
(Principal Financial Officer) |
43
EXHIBIT 2.1
CERTAIN PORTIONS OF THIS EXHIBIT (INDICATED BY [***]) HAVE BEEN EXCLUDED PURSUANT TO ITEM 601(B)(10) OF REGULATION S-K BECAUSE THEY ARE BOTH NOT MATERIAL AND ARE THE TYPE THAT THE COMPANY TREATS AS PRIVATE AND CONFIDENTIAL.
THIS FIRST AMENDMENT TO AMENDED AND RESTATED COLLABORATION AND COMMERCIALIZATION AGREEMENT (this “Amendment”) is entered into as of March 12, 2026 (the “Amendment Effective Date”) by and between Senseonics, Incorporated, a Delaware corporation (“Senseonics”) and Ascensia Diabetes Care Holdings AG (“Ascensia”).
RECITALS
WHEREAS, Senseonics and Ascensia have entered into that certain Amended and Restated Collaboration and Commercialization Agreement, dated December 31, 2025 (the “Agreement”); and
WHEREAS, the parties desire to amend the Agreement as set forth herein.
NOW, THEREFORE, in consideration of the mutual promises and covenants herein and other consideration, the receipt and sufficiency of which is hereby acknowledged, the parties hereby agree as follow:
AGREEMENT
“Tender Agreement” means any agreement with respect to Italy, Spain and/or Sweden, between Ascensia and any local or regional governmental entity or governmental body for the Supply of Products in the Field to a pre-defined user group.
Promotional Materials. Senseonics will be responsible for reviewing and approving key advertising, sales information, literature, and other promotional materials pertaining Products (“Promotional Material”) prior to use or dissemination by Ascensia in the Territories. Senseonics is fully responsible for ensuring all new materials are compliant according to relevant legal, medical, and regulatory standards. Notwithstanding the foregoing, any Promotional Materials that are in use by Ascensia in the Territory as of the Amended Effective Date and have been previously approved by Senseonics (if and to the extent such approval was required under the Prior Agreement) may continue to be used by Ascensia without further review or approval by Senseonics, so long as they remain accurate, compliant with applicable law and consistent with this Agreement.
4.3 Taxes. Unless otherwise provided on the Purchase Order, in addition to the amounts stated above, Senseonics shall pay costs for all sales, use, value-added or excise taxes, assessments or other charges, including customs duties and similar fees attributable to the sale of the Product. In the event Ascensia pays any such fees, taxes, or charges, Ascensia shall promptly invoice Senseonics for the same pursuant to the Transition Services Agreement, except that duties import are to be included in the COGS per section 4.4 and settled through the corresponding true-up.
4.4 Transition True-up. For the period from [***], or [***], the Parties shall conduct a monthly true-up to account for [***]. For such true-up, the amounts owed to Senseonics under the 100% revenue share shall be reduced to the extent of [***], to the extent that (i) such amounts are actually incurred and paid out in the period and (ii) such amounts are not otherwise attributable to or accounted for under the Transition Services Agreement, including without limitation under Schedule A cost sharing, Schedule B, payments for operating expenses, or otherwise.
[Signature Page Follows]
IN WITNESS WHEREOF, the parties confirm and acknowledge the terms of this Agreement. The parties represent and warrant that the persons executing this Amendment have all necessary authority to enter into, and bind the relevant entity, to this Amendment.
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Senseonics: Senseonics, Incorporated Signature: /s/ Timothy T. Goodnow, Ph.D. Name: Timothy T. Goodnow, Ph.D. Title: President and CEO Date: March 12, 2026 |
Ascensia: Ascensia Diabetes Care Holdings AG Signature: Name: Title: Date: Signature: Name: Title: Date: |
IN WITNESS WHEREOF, the parties confirm and acknowledge the terms of this Agreement. The parties represent and warrant that the persons executing this Amendment have all necessary authority to enter into, and bind the relevant entity, to this Amendment.
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Senseonics: Senseonics, Incorporated Signature: Name: Title: Date: |
Ascensia: Ascensia Diabetes Care Holdings AG Signature: /s/ Koichiro Sato Name: Koichiro Sato Title: Chief Executive Officer Date: 3/11/2026 Signature: /s/ Marieke Jansen Name: Marieke Jansen Title: General Counsel Date: 3/11/2026 |
EXHIBIT 2.2
CERTAIN PORTIONS OF THIS EXHIBIT (INDICATED BY [***]) HAVE BEEN
EXCLUDED PURSUANT TO ITEM 601(B)(10) OF REGULATION S-K BECAUSE THEY
ARE BOTH NOT MATERIAL AND ARE THE TYPE THAT THE COMPANY TREATS
AS PRIVATE AND CONFIDENTIAL.

LOCAL ASSET PURCHASE AGREEMENT
among:
Senseonics Sweden AB (hereinafter the “Purchaser Affiliate”)
Ascensia Diabetes Care Holdings AG (hereinafter the “Seller Parent”)
and
Ascensia Diabetes Care Sweden AB (hereinafter the “Seller Affiliate”)
Dated as of March 12, 2026

THIS LOCAL ASSET PURCHASE AGREEMENT (the “Agreement”), dated as of March 12, 2026, is by and among, ASCENSIA DIABETES CARE HOLDINGS AG, a company organized under the laws of Switzerland (hereinafter “Seller Parent”), Ascensia Diabetes Care Sweden AB, reg. no. 559024-5345, a limited liability company incorporated in Sweden, with address at Gustav III Boulevard 34, 169 73 Solna, Sweden (the “Seller Affiliate” and together with Seller Parent, the “Seller Parties”) and Senseonics Sweden AB, reg. no. 559549-6026, a limited liability company incorporated under the laws of Sweden, with address at c/o Athene Tax AB Textilgatan 31, 120 30 Stockholm, Sweden (the “Purchaser Affiliate”). Any capitalized terms used in this Agreement and not herein defined shall have the meaning assigned to such terms in the Master Purchase Agreement attached hereto as Annex A.
Preamble
A.Seller Parent, which is the ultimate parent company of the Seller Affiliate, and Senseonics, Incorporated, a Delaware corporation (hereinafter “Purchaser Parent”), the ultimate parent company of the Purchaser Affiliate have entered into a Master Asset Purchase Agreement, dated December 31, 2025 (as may be amended from time to time, the “Master Purchase Agreement”), pursuant to which, among other things, Seller Parent agreed to sell or cause one or more of its Affiliates (including Seller Affiliate), to sell to Purchaser Parent or one or more of its Affiliates (including Purchaser Affiliate), certain CGM Activities (as defined in the Master Purchase Agreement) in particular through the sale of certain assets of certain affiliates of Seller Parent.
B.Seller Affiliate owns the right, title and interest to the Specified European Assets located in Sweden representing its business (going concern) of marketing, selling and distributing the Products in Sweden (collectively, the “Sweden Purchased Assets”) and desires to sell them to Purchaser Affiliate, and Purchaser Affiliate wishes to purchase from Seller Affiliate, the Sweden Purchased Assets and, in connection therewith, Purchaser Affiliate is willing to assume the Sweden Assumed Liabilities (as defined below) (the Sweden Assumed Liabilities together with the Sweden Purchased Assets, collectively, the “Sweden Business”), in each case, upon the terms and subject to the conditions set forth in this Agreement and the Master Purchase Agreement.
NOW, THEREFORE, in consideration of the foregoing and the respective representations, warranties, covenants, agreements and conditions set forth in this Agreement and the Master Purchase Agreement, the Parties agree as follows:
Unless otherwise expressly stated in this Agreement, terms used but not defined herein shall have the meanings assigned to them in the Master Purchase Agreement. The following terms, used in this Agreement, have the following meanings:
“Applicable Law” means any law, statute, legislation, ordinance, code, rule or regulation, including any EU regulation, treaty or international agreement, as well as any judgment, order, injunction, ruling, decision or other legally binding requirement of any court, tribunal, governmental, regulatory or supervisory authority, in each case as in force and applicable to the relevant Person from time to time.
“Closing” shall mean the consummation of the transactions set forth in Section 4 of this Agreement.
“Closing Date” shall mean the date of Closing as provided for in Section 4 of this Agreement.
“Encumbrances” shall mean any pledge (Sw. panträtt), enterprise mortgage (Sw. företagshypotek), mortgage (Sw. inteckning), security interest, encumbrance, claim, preference, right of possession, lease, tenancy, license, easement (Sw. servitut), restrictive covenant, infringement, interference, court order, proxy, option, right of first refusal, pre-emptive right, defect, impediment, exception, reservation, limitation, impairment, imperfection of title, condition or restriction of any nature (including any restriction on the transfer of any asset, any restriction on the receipt of any income derived from any asset, any restriction on the use of any asset and any restriction on the possession, exercise or transfer of any other attribute of ownership of any asset), right of use or usufruct (Sw. nyttjanderätt), retention of title (Sw. äganderättsförbehåll), mandatory transfer right / right of first offer (Sw. hembud) and any other third party right.
“Master Purchase Agreement” has the meaning set forth in Preamble A.
“Material Adverse Change” means any event, change, circumstance or effect that, individually or in the aggregate, has a material adverse effect on the Sweden Purchased Assets.
“Purchaser Parent” has the meaning set forth in Preamble A.
“Products” shall mean the following Purchaser proprietary products currently marketed under the brand “Eversense”: (a) Eversense® CGM System (90-day product); (b) Eversense® XL CGM System (180-day product outside the US); (c) Eversense XL 2.0; and (d) extended Eversense 365-day product (Rome 1 & Rome 2).
“Seller Parent” has the meaning set forth in Preamble A.
“Sweden Assumed Liabilities” has the meaning set forth in Section 2.3.
“Sweden Business” has the meaning set forth in Preamble B.
“Sweden Excluded Assets” has the meaning set forth in Section 2.2.
“Sweden Purchased Assets” has the meaning set forth in Preamble B.
“Sweden Purchase Price” has the meaning set forth in Section 3.
“Sweden Transferred Employees” has the meaning set forth in Section 2.5.
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| 5. | Closing Conditions. |
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[Signature Page Follows.]
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IN WITNESS WHEREOF, the Parties hereto have executed this Agreement as of the date first written above.
Ascensia Diabetes Care Holdings AG
(two signatories required)
By: /s/ Koichiro Sato
Name: Koichiro Sato
Title: Chief Executive Officer
Ascensia Diabetes Care Holdings AG
(two signatories required)
By: /s/ Marieke Jansen
Name: Marieke Jansen
Title: General Counsel
[Signature Page to Local Asset Purchase Agreement (Sweden)]
IN WITNESS WHEREOF, the Parties hereto have executed this Agreement as of the date first written above.
PURCHASER AFFILIATE:
Senseonics Sweden AB
By: /s/ Timothy T. Goodnow, Ph.D.
Name: Timothy T. Goodnow, Ph.D.
Title: Director
By: /s/ Rick Sullivan
Name: Rick Sullivan
Title: Director
[Signature Page to Local Asset Purchase Agreement (Sweden)]
Schedule 1
Sweden Purchased Assets
[***]
Schedule 2
Tender Contracts
[***]
Schedule 2.2
Sweden Excluded Assets
[***]
Schedule 2.5
Sweden Transferred Employees
[***]
Schedule 3
Other Sweden Transferred Contracts
[***]
EXHIBIT 2.3
CERTAIN PORTIONS OF THIS EXHIBIT (INDICATED BY [***]) HAVE BEEN EXCLUDED PURSUANT TO ITEM 601(B)(10) OF REGULATION S-K BECAUSE THEY ARE BOTH NOT MATERIAL AND ARE THE TYPE THAT THE COMPANY TREATS AS PRIVATE AND CONFIDENTIAL.
BUSINESS TRANSFER AGREEMENT
Senseonics Spain S.L.U.
and
Ascensia Diabetes Care Spain, S.L.U.
Dated as of March 12, 2026
TABLE OF CONTENTS
Page
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THIS BUSINESS TRANSFER AGREEMENT (the “Agreement”), dated as of March 12, 2026, is by and between ASCENSIA DIABETES CARE SPAIN, S.L.U., incorporated under the laws of Spain, with registered office address at Pz de la Pau, s/n, WTC Alameda Park Ed.6, 3 Planta, Cornella de Llobregat, Barcelona (Spain), with Spanish Tax ID number B87346433 and duly registered with the Commercial Registry of Barcelona under volume 45,406, sheet 29, page B-486684 (the “Seller Affiliate”), duly represented by [***], as Sole Director of the Seller Affiliate by virtue of the public deed granted before the Notary Public, Mr. J.V.Torres Montero, on November 6, 2011, number 3,120 of his protocol and duly registered with the Commercial Registry of Barcelona under entry 11; and SENSEONICS SPAIN S.L.U., incorporated under the laws of Spain, with registered office address at C/ Muntaner 239, Ático, 08021 Barcelona (Spain), with Spanish Tax ID number B24798324 and duly registered with the Commercial Registry of Barcelona under page B-645444 (the “Purchaser Affiliate”) duly represented by [***], in force, as joint and several director of the Purchaser Affiliate by virtue of the public deed granted before the Notary Public, Mr. I. Molinos Gil, on November 5, 2025, number 5,834 of his protocol and duly registered with the Commercial Registry of Barcelona under entry 1. Hereinafter, the Seller Affiliate and the Purchaser Affiliate shall be jointly referred to as the “Parties” and each of them a “Party”.
Preamble
A.ASCENSIA DIABETES CARE HOLDINGS AG, a company organized under the laws of Switzerland (hereinafter “Seller Parent”), which is the ultimate parent company of the Seller Affiliate, and SENSEONICS, INCORPORATED, a Delaware corporation (hereinafter “Purchaser Parent”), the ultimate parent company of the Purchaser Affiliate have entered into a Master Asset Purchase Agreement, dated December 31, 2025 (as may be amended from time to time, the “Master Purchase Agreement”), pursuant to which, among other things, Seller Parent agreed to sell, or cause one or more of its Affiliates (including Seller Affiliate), to sell to Purchaser Parent or one or more of its Affiliates (including Purchaser Affiliate), certain CGM Activities (as defined in the Master Purchase Agreement) in particular through the sale of certain assets of certain affiliates of Seller Parent (the “Global Transaction”). A copy of the executed Master Purchase Agreement is attached hereto as Annex I. Any capitalized terms used in this Agreement and not herein defined shall have the meaning assigned to such terms in the Master Purchase Agreement.
B.The Seller Parent’s main activity is, among others, the business of marketing, selling and distributing the Products in the Territory (the “Business”). The Seller Parent indirectly carries out the Business in Spain through the Seller Affiliate who owns the right, title and interest to the Spain Purchased Assets (including the Spain Transferred Contracts), the Spain Assumed Liabilities and the Transferred Employees (as each term is defined below).
C.Seller Affiliate owns the right, title and interest to the Specified European Assets located in Spain (the “Spain Purchased Assets”) which, together with the Spain Assumed Liabilities and Transferred Employees, represent its business (going concern) of marketing, selling and distribution of the Products in Spain (the “Spain Business”). Seller Affiliate desires to sell the Spain Business to Purchaser Affiliate, and Purchaser Affiliate wishes to purchase from Seller Affiliate, the Spain Business, upon the terms and subject to the conditions set forth in this Agreement and the Master Purchase Agreement.
D.On [***], the Seller Affiliate has notified the Transferred Employees’ (as this term is defined below) workers’ representatives, that, within the context of the Global Transaction, the labor contracts of the Transferred Employees, will be assigned in favor of the Purchaser Affiliate. A copy of such notification is attached hereto as Schedule (D).
E.In the context of the Global Transaction and in accordance with the Master Purchase Agreement, the Seller Affiliate desires to sell, transfer and assign to the Purchaser Affiliate, and the Purchaser Affiliate desires to purchase, acquire and assume from the Seller Affiliate, as a going concern, the Spain Business upon the terms and subject to the conditions set forth in this Agreement and the provisions of the Master Purchase Agreement.
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NOW, THEREFORE, in consideration of the foregoing and the respective representations, warranties, covenants, agreements and conditions set forth in this Agreement, the Parties agree as follows:
“Agreement” means this agreement.
“Business” has the meaning ascribed to such term at the Preamble.
“Closing Conditions” has the meaning ascribed to such term in Clause 5.
“Closing Date”has the meaning ascribed to such term in Clause 4.
“Closing” has the meaning ascribed to such term in Clause 4.
“Excluded Assets” shall mean any asset not transferred as per the terms and conditions of this Agreement and/or the Master Purchase Agreement.
“Global Transaction” has the meaning ascribed to such term at the Preamble.
“Master Purchase Agreement” has the meaning ascribed to such term at the Preamble.
“Party” or “Parties” has the meaning ascribed to such term at the Preamble.
“Person” shall mean any individual, entity or governmental body.
“Products” shall mean the following proprietary products of Purchaser Parent currently marketed under the brand “Eversense”: (a) Eversense® CGM System (90-day product); (b) Eversense® XL CGM System (180-day product outside the US); and (c) Eversense XL 2.0; (d) extended Eversense 365-day product (Rome 1 & Rome 2).
“Public Sector Contracts Law” has the meaning ascribed to such term in Clause 5.1.1(b).
“Purchaser Affiliate” has the meaning ascribed to such term at the Preamble.
“Purchaser Parent” has the meaning ascribed to such term at the Preamble.
“Seller Affiliate” has the meaning ascribed to such term at the Preamble.
“Seller Group”shall mean the Seller Parent and its Affiliates.
“Seller Parent” has the meaning ascribed to such term at the Preamble.
“Spain Assumed Liabilities” has the meaning ascribed to such term in Clause 2.1.3.
“Spain Business” has the meaning ascribed to such term at the Preamble.
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“Spain Purchase Price” has the meaning ascribed to such term in Clause 3.1.
“Spain Purchased Assets” has the meaning ascribed to such term at the Preamble.
“Spain Tender Contracts” has the meaning ascribed to such term in Clause 6.2.1(a).
“Spain Transferred Contracts” has the meaning ascribed to such term in Clause 2.1.1(b).
“Spain Transferred Employees” has the meaning ascribed to such term in Clause 2.1.5.
“Spanish Workers Statute” has the meaning ascribed to such term in Clause 7.
“Additional TUPE Notification” has the meaning ascribed to such term in Clause 7.4.
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For clarification purposes, the Parties expressly state that the Seller Affiliate transfers and the Purchaser Affiliate acquires all the above elements forming part of the Spain Business as a whole. This means that they are transferred as integral parts of a functioning production unit (unidad productiva) that can continue to be operated autonomously and independently, and not each of them as separate and individually considered elements or objects.
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For clarification purposes, it is hereby stated that (i) the Closing Conditions suspend the obligation to proceed with the Closing until they are fulfilled, but do not suspend the effectiveness of the other obligations established in this Agreement, the Transition Services Agreement and the Master Purchase Agreement, which shall take full effect from the moment of its signing; and (ii) the Closing Conditions are established in favor of the Purchaser Affiliate, who may waive its fulfilment prior to the long-stop date referred to in Section 5 above.
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Notice to the Purchaser Affiliate: Senseonics Spain S.L.U. c/o Senseonics Holdings, Inc. |
Notice to the Seller Affiliate: Ascensia Diabetes Care Spain S.L.U. |
Attention: [***] |
Attention: [***] |
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Address: 20451 Seneca Meadows Parkway Germantown, MD 20876-7005 |
Address: Pz de la Pau, s/n, WTC Alameda Park Ed.6, 3 Planta, Cornella de Llobregat, Barcelona (Spain) |
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Email: [***] With cc to: Cooley LLP 11951 Freedom Drive |
Email: [***] |
With cc to: [***] |
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Address: Peter Merian-Strasse 90 4052 Basel, Switzerland |
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Notice to the Purchaser Affiliate: Senseonics Spain S.L.U. c/o Senseonics Holdings, Inc. |
Notice to the Seller Affiliate: Ascensia Diabetes Care Spain S.L.U. |
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14th Floor Reston, VA 20190-5656 Attn: [***] Email: [***] |
Email: [***] |
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[Signature Page Follows.]
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IN WITNESS WHEREOF, the Parties hereto have executed this Agreement as of the date first written above.
SELLER AFFILIATE:
Ascensia Diabetes Care Spain, S.L.U.
/s/ María Gemma Pérez Cambra
Name: Mrs. María Gemma Pérez Cambra Name: Timothy Todd Goodnow, Ph.D.
Title: Sole Director
[Signature Page to Business Purchase Agreement (Spain)]
IN WITNESS WHEREOF, the Parties hereto have executed this Agreement as of the date first written above.
PURCHASER AFFILIATE:
Senseonics Spain S.L.
By: /s/ Timothy Todd Goodnow, Ph.D.
Title: Joint and Several Director (Annex A was omitted because it was previously filed as Exhibit 2.1 to the Company’s 2025 Form 10-K filed with the Securities and Exchange Commission on March 2, 2026).
[Signature Page to Business Purchase Agreement (Spain)]
Annex A
Master Purchase Agreement
[***]
Schedule D
Spain Notification of Transferred Employees’ workers’ representatives
[***]
Schedule 2.1.1(a)
Spain Purchased Assets
[***]
Schedule 2.1.1(b)-I
Spain Tender Contracts
[***]
Schedule 2.1.1(b)-II
Other Spain Transferred Contracts
[***]
Schedule 2.1.5
Spain Transferred Employees
[***]
Schedule 5.1.1(b)
Tender Contracts Communication
[***]
Schedule 6.2.1(d)
After Closing Communication to Tenders
[***]
Schedule 7.4
Additional TUPE Notification
[***]
EXHIBIT 2.4
CERTAIN PORTIONS OF THIS EXHIBIT (INDICATED BY [***]) HAVE BEEN EXCLUDED PURSUANT TO ITEM 601(B)(10) OF REGULATION S-K BECAUSE THEY ARE BOTH NOT MATERIAL AND ARE THE TYPE THAT THE COMPANY TREATS AS PRIVATE AND CONFIDENTIAL.

LOCAL ASSET PURCHASE AGREEMENT
among:
Senseonics, Incorporated (hereinafter “Purchaser Parent”), Senseonics Deutschland GmbH (hereinafter the “Purchaser Affiliate”), Ascensia Diabetes Care Holdings AG (hereinafter the “Seller Parent”),
and
Ascensia Diabetes Care Deutschland GmbH (hereinafter the “Seller Affiliate”)


Dated as of March 12, 2026

TABLE OF CONTENTS
Page
i
THIS LOCAL ASSET PURCHASE AGREEMENT (the “Agreement”), dated as of March 12, 2026 (the “Signing Date”), is by and among Ascensia Diabetes Care Holdings AG, a company organized under the laws of Switzerland (hereinafter “Seller Parent”), which is the ultimate parent company of the Seller Affiliate, Ascensia Diabetes Care Deutschland GmbH, a limited liability company (Gesellschaft mit beschränkter Haftung) incorporated in Leverkusen, registered with the commercial register of the local court of Cologne under HRB 86819 and registered business address at Marie-Curie-Strasse 5, 51377 Leverkusen Germany (the “Seller Affiliate” and together with Seller Parent, the “Seller Parties”), Senseonics, Incorporated, a Delaware corporation (hereinafter “Purchaser Parent”), the ultimate parent company of the Purchaser Affiliate and Senseonics Deutschland GmbH, a limited liability company (Gesellschaft mit beschränkter Haftung) incorporated under the Laws of Germany, registered with the commercial register of the local court of Munich under HRB 307667 and registered business address at Erika-Mann-Straße 63, 80636 Munich (the “Purchaser Affiliate” and together with Purchaser Parent, the “Purchaser Parties”). The Purchaser Parties and Seller Parties are collectively referred to herein the “Parties” and each of them a “Party”. Any capitalized terms used in this Agreement and not herein defined shall have the meaning assigned to such terms in the Master Purchase Agreement attached hereto as Annex A.
Preamble
NOW, THEREFORE, in consideration of the foregoing and the respective representations, warranties, covenants, agreements and conditions set forth in this Agreement and the Master Purchase Agreement, the Parties agree as follows:
“Closing” shall mean the consummation of the transactions set forth in Section 4 of this Agreement.
“Closing Date” shall mean the date of Closing as provided for in Section 4 of this Agreement.
“Products” shall mean the following Purchaser proprietary products currently marketed under the brand “Eversense”: (a) Eversense® CGM System (90-day product); (b) Eversense® XL CGM System (180-day product outside the US); (c) Eversense XL 2.0; (d) Eversense E3, if it´s not already covered by Eversense XL 2.0 and (e) extended Eversense 365-day product (Rome 1 & Rome 2).
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[Signature Page Follows.]
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IN WITNESS WHEREOF, the Parties hereto have executed this Agreement as of the date first written above.
SELLER AFFILIATE: |
Ascensia Diabetes Care Deutschland GmbH |
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/s/ Matthew Stewart |
Name: Matthew Stewart |
Title: Managing Director of Germany / Commercial Leader DACH and Poland |
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SELLER PARENT: |
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Ascensia Diabetes Care Holdings AG |
(two signatories required) |
By: /s/ Koichiro Sato |
Name: Koichiro Sato |
Title: Chief Executive Officer |
Ascensia Diabetes Care Holdings AG |
(two signatories required) |
By: /s/ Marieke Jansen |
Name: Marieke Jansen |
Title: General Counsel |
[Signature Page to Local Asset Purchase Agreement (Germany)]
IN WITNESS WHEREOF, the Parties hereto have executed this Agreement as of the date first written above.
PURCHASER AFFILIATE: |
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Senseonics Deutschland GmbH |
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By: /s/ Timothy T. Goodnow, Ph.D. Name: Timothy T. Goodnow, Ph.D. |
Title: Director |
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By: /s/ Rick Sullivan |
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Name: Rick Sullivan |
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Title: Director |
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PURCHASER PARENT: |
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Senseonics, Incorporated |
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By: /s/ Timothy T. Goodnow, Ph.D. |
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Name: Timothy T. Goodnow, Ph.D. |
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Title: President and CEO |
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[Signature Page to Local Asset Purchase Agreement (Germany)]
Annex A
Master Purchase Agreement
[***]
(Annex A was omitted because it was previously filed as Exhibit 2.1 to the Company’s Form 10-K for the fiscal year ended December 31, 2025 filed with the Securities and Exchange Commission on March 2, 2026).
EXHIBIT 2.5
CERTAIN PORTIONS OF THIS EXHIBIT (INDICATED BY [***]) HAVE BEEN
EXCLUDED PURSUANT TO ITEM 601(B)(10) OF REGULATION S-K BECAUSE THEY
ARE BOTH NOT MATERIAL AND ARE THE TYPE THAT THE COMPANY TREATS
AS PRIVATE AND CONFIDENTIAL.
DEED OF TRANSFER OF BUSINESS
between:
Senseonics Italy S.r.l. (hereinafter the “Purchaser Affiliate”)
and
Ascensia Diabetes Care Italy S.r.l. (hereinafter the “Seller Affiliate”)
Dated as of March 10, 2026
THIS DEED OF TRANSFER OF BUSINESS (the “Agreement”), dated as of March 10, 2026, is by and between Ascensia Diabetes Care Italy S.r.l., a limited liability company incorporated in Italy, having its registered office in Milan, at Via Varesina n. 162, tax code and registration number with the Register of Enterprises of Milan Monza Brianza Lodi no. 13522771008, represented by Aldo Saetta, [***], acting in the present deed in his capacity as Manager of Finance and Controlling and duly empowered by virtue of resolution of the quotaholders’ meeting (the “Seller Affiliate”) and Senseonics Italy S.r.l., a limited liability company incorporated under the laws of Italy, having its registered office in Milan, Via Michelangelo Buonarroti no. 39, tax code and registration number with the Register of Enterprises of Milan Monza Brianza Lodi no. 14430890963, represented by (a) Timothy T. Goodnow, [***] and (b) Frederick Thomas Sullivan, [***], each acting in the present deed in his capacity as director and duly empowered by virtue of Purchaser Affiliate’s by-laws (the “Purchaser Affiliate” and, jointly with the Seller Affiliate, the “Parties” and each of them a “Party”). Any capitalized terms used in this Agreement and not herein defined shall have the meaning assigned to such terms in the Master Purchase Agreement (as defined below).
Preamble
A.The Seller Affiliate is an Italian limited liability company active in the development, production, marketing and sale in the medical and healthcare sector, including diagnostic devices and services.
B.The Purchaser Affiliate is an Italian limited liability company active in the information technology applied to healthcare field.
C.ASCENSIA DIABETES CARE HOLDINGS AG, a company organized under the laws of Switzerland (hereinafter “Seller Parent”), which is the ultimate parent company of the Seller Affiliate, and SENSEONICS, INCORPORATED, a Delaware corporation (hereinafter “Purchaser Parent”), the ultimate parent company of the Purchaser Affiliate have entered into a Master Asset Purchase Agreement, dated December 31, 2025 (as may be amended from time to time, the “Master Purchase Agreement”), pursuant to which, among other things, Seller Parent agreed to sell, or cause one or more of its Affiliates (including Seller Affiliate), to sell to Purchaser Parent or one or more of its Affiliates (including Purchaser Affiliate), certain CGM Activities (as defined in the Master Purchase Agreement) in particular through the sale of certain assets of certain affiliates of Seller Parent. A copy of the executed Master Purchase Agreement is attached hereto as Schedule D.
D.Seller Affiliate owns the right, title and interest to the Specified European Assets located in Italy representing its business (going concern) of marketing, selling and distributing the Products in Italy (collectively, the “Italy Purchased Assets”) and desires to sell them to Purchaser Affiliate, and Purchaser Affiliate wishes to purchase from Seller Affiliate, the Italy Purchased Assets and, in connection therewith, Purchaser Affiliate is willing to assume the Italy Assumed Liabilities (jointly with the Italy Purchased Assets, the “Italy Business”), in each case, upon the terms and subject to the conditions set forth in this Agreement and the Master Purchase Agreement.
E.Pursuant to Law Decree 21/2012 converted by Law No. 56 of 11 May 2012, as amended and supplemented from time to time, and its implementing regulation and decrees ("Golden Power Law"), following notification of the acquisition of the Italy Business made by the Parties on 18 December 2025, the Presidency of the Italian Council of Ministers (Presidenza del Consiglio dei Ministri), by communication dated 30 January 2026 (Proceeding No. 860/2025 - DICAGP-0000766), notified the Parties that the transaction, as notified, does not fall within the scope of the Golden Power Law.
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NOW, THEREFORE, in consideration of the foregoing and the respective representations, warranties, covenants, agreements and conditions set forth in this Agreement and the Master Purchase Agreement, the parties agree as follows:
“Closing” shall mean the transfer of the legal ownership of the Italy Business to the Purchaser Affiliate, pursuant to Section 2 of this Agreement, and, in general, the execution of the notarial deed of transfer of the Italy Business and exchange of all documents and agreements and the performance and consummation of all the obligations and transactions required to be executed, exchanged, performed or consummated on the Closing Date pursuant to this Agreement.
“Closing Date” shall mean the date of execution of the notarial deed of transfer of the Italy Business before the Italian notary selected by the Purchaser Affiliate substantially in the form attached hereto as Schedule C.
“Products” shall mean the following Purchaser proprietary products currently marketed under the brand “Eversense”: (a) Eversense® CGM System (90-day product); (b) Eversense® XL CGM System (180-day product outside the US); (c) Eversense XL 2.0; and (d) extended Eversense 365-day product (Rome 1 & Rome 2).
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| (a) | applicable Law; and/or |
| (b) | any decision, interpretation or requirement of the relevant contracting authority; and/or |
| (c) | any characteristic, act, omission or circumstance relating to the Purchaser Affiliate, including the absence of any eligibility, qualification or other general and special requirements prescribed under applicable Law, it being understood that the Purchaser Affiliate shall use reasonable best efforts to independently obtain such requirements. |
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| (a) | The Purchaser Affiliate is duly organized and validly existing under the laws of the jurisdiction of its incorporation or formation. |
| (b) | The Purchaser Affiliate has the requisite corporate or similar power to execute and deliver this Agreement, to perform its obligations hereunder and to consummate the transactions contemplated hereby. The execution and delivery by the Purchaser Affiliate of this Agreement, the performance by the Purchaser Affiliate of its obligations hereunder and the consummation by the Purchaser Affiliate of the transactions contemplated hereby have been duly and validly authorized by all necessary organizational action with respect to the Purchaser Affiliate, each such authorization remains in full force and effect and no other corporate proceedings on the part of the Purchaser Affiliate are necessary therefor. |
| (c) | This Agreement has been duly executed and delivered by the Purchaser Affiliate and, assuming the due execution hereof by the Seller Affiliate, this Agreement constitutes a legal, valid and binding obligation of the Purchaser Affiliate, enforceable against the Purchaser Affiliate in accordance with its terms, except to the extent enforceability may be limited by any applicable bankruptcy, reorganization, insolvency, moratorium or other similar applicable laws affecting the rights of creditors generally. |
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*****
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Schedule A
Italy Purchased Assets
[***]
Schedule B
Italy Transferred Employees
[***]
Schedule C
Notarial Deed of Transfer
[***]
Schedule D
Master Asset Purchase Agreement
[***]
(Schedule D was omitted because it was previously filed as Exhibit 2.1 to the Company’s Form 10-K for the fiscal year ended December 31, 2025 filed with the Securities and Exchange Commission on March 2, 2026).
*****
Should the above reflect the content of understandings reached and intentions shared, if you agree on the above terms and conditions, please notify us of Your acceptance by returning us a copy of this Proposal initialised on each page and undersigned for acceptance.
Kind regards,
Senseonics Italy S.r.l.
Acting by their authorised signatories:
|
/s/ Timothy T. Goodnow Name: Timothy T. Goodnow Title: Director |
/s/ Frederick Thomas Sullivan Name: Frederick Thomas Sullivan Title: Director |
*****
I hereby fully and unconditionally confirm our acceptance to your Proposal, according to the terms and conditions above.
Kind regards,
Ascensia Diabetes Care Italy S.r.l.
Acting by its authorised signatory:
/s/ Aldo Saetta
Name: Aldo Saetta
EXHIBIT 10.2
CERTAIN PORTIONS OF THIS EXHIBIT (INDICATED BY [***]) HAVE BEEN EXCLUDED PURSUANT TO ITEM 601(B)(10) OF REGULATION S-K BECAUSE THEY ARE BOTH NOT MATERIAL AND ARE THE TYPE THAT THE COMPANY TREATS AS PRIVATE AND CONFIDENTIAL.
Execution Version
TRANSITION SERVICES AGREEMENT
Title: Manager of Finance and Controlling This TRANSITION SERVICES AGREEMENT (this “Agreement”) is made and entered into as of March 12, 2026, (the “Effective Date”) by and among Senseonics, Incorporated (“Buyer”), Ascensia Diabetes Care Holdings AG and the European Ascensia Affiliates (collectively, “Ascensia”) (each a, “Party” and together, the “Parties”). Capitalized terms used but not defined in this Agreement shall have the meaning given to them in the Purchase Agreement (as defined below).
RECITALS
A.Buyer and Ascensia have entered into that certain Master Asset Purchase Agreement, dated as of December 31, 2025 (as amended and supplemented, the “Purchase Agreement”) to consummate the sale of the Specified Initial Assets and U.S. CGM Activities to Buyer and are concurrently herewith negotiating and finalizing the respective Local Purchase Agreements to consummate the sale of the Specified European Assets and European CGM Activities in the European Selected Territories to the applicable Purchaser Affiliate.
B.Concurrently with initiation of the Transition Services under this Agreement, the Parties to the Purchase Agreement are consummating an agreement for the sale of the Specified European Assets and European CGM Activities in the European Selected Territories to the applicable Purchaser Affiliate as contemplated by the applicable Local Purchase Agreement.
C.In connection with the transactions contemplated by the Purchase Agreement and Ascensia’s obligations under the Purchase Agreement, Ascensia desires to provide Buyer with, and Buyer desires to receive, certain services in the Selected Territories in Europe to provide for the continuity of the business in the Selected Territories through the sales process as contemplated by the Purchase Agreement, including the continuation of commercial operations in a manner consistent with Performance Standards, including with respect to performance under Tender Contracts, IT and systems migration, Business employee support, finance and operations support, regulatory compliance, and other agreed services, in each case, throughout the respective periods set forth below, subject to the terms and conditions set forth in this Agreement and the applicable Schedules attached hereto.
D.In connection with the transactions contemplated by the Purchase Agreement, Ascensia desires to provide Buyer with, and Buyer desires to receive, certain transition services after the Closings in the Selected Territories in Europe to ensure an orderly and uninterrupted transition of the Business from Ascensia to Buyer, including the continuation of commercial operations in a manner consistent with Performance Standards, including with respect to performance under Tender Contracts, IT and systems migration, CGM employee support, finance and operations support, regulatory compliance, and other agreed services, in each case, throughout the respective periods set forth below, subject to the terms and conditions set forth in this Agreement and the applicable Schedules attached hereto.
E.It is the goal of the Parties that the covenants, terms and conditions of the Purchase Agreement and this Agreement will support the preservation of the value of the Business, the preparation of the Business for transition to Buyer, and an orderly and uninterrupted transition of the Business from Ascensia to Buyer; provided, however, that nothing in these Recitals shall be deemed to expand or modify the Performance Standard or the scope of the Transition Services beyond those expressly set forth in this Agreement and the Schedules (together with any Ancillary Services).
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NOW, THEREFORE, in consideration of the covenants, promises and representations set forth in this Agreement, and for other good and valuable consideration, the receipt and sufficiency of which are hereby acknowledged, the Parties agree as follows:
All capitalized terms used but not specifically defined in this Agreement have the meanings assigned to them in the Purchase Agreement.
| 1.1 | “Affiliates” shall have the meaning set forth in the Purchase Agreement. |
| 1.2 | “Ancillary Services” means activities inherently necessary to perform a Service expressly described in Schedules A – D attached hereto that do not otherwise materially increase scope, complexity, or cost and that are materially consistent with how such Services are currently being performed by Ascensia as of the Effective Date. |
| 1.3 | “Business” means Ascensia’s Eversense CGM business in the Selected Territories. |
| 1.4 | “Buyer Approver Overage” means CGM Direct Operating Costs in excess of the applicable line item in the Operating Budget but not exceeding [***]. |
| 1.5 | “CGM Direct Operating Costs” means direct operating costs and expenses that are reasonably necessary to be incurred and are actually incurred in connection with the performance of the Transition Services or operation of the Business in the European Selected Territories, including, without limitation, third party vendor charges, logistics, tender fees, and travel (in accordance with Ascensia’s policies), but excluding personnel costs and any costs that are duplicative of items already captured within TSA Fees or otherwise not reasonably necessary for the performance of the Transition Services or operation of the Business in the European Selected Territories. |
| 1.6 | “Closing(s)” shall have the meaning as set forth in the Purchase Agreement. |
| 1.7 | “Collaboration Agreement” means that certain Amended and Restated Collaboration Agreement, dated as of the Effective Date, between the Parties, as it may be amended and/or further restated from time to time. |
| 1.8 | “Establishment Activities” means activities necessary for Buyer to establish operational control over, and conduct, the Business in Selected Territories, including entity formation, Tender Contract transfers, order to cash process establishment, CRM and IT transition, regulatory compliance, back-office set-up, and employee processes and onboarding. |
| 1.9 | “European Ascensia Affiliates” means Ascensia Diabetes Care Deutschland GmbH, Ascensia Diabetes Care Italy Srl., Ascensia Diabetes Care Spain SL., and Ascensia Diabetes Care Sweden AB. |
| 1.10 | “European Selected Territories” means Selected Territories other than the U.S. |
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| 1.11 | “Excluded Territories” means Poland, Switzerland and all other geographies that are not Selected Territories. |
| 1.12 | “Force Majeure Event” means any event or circumstance beyond the reasonable control of the affected Party that prevents or delays performance of its obligations, despite the affected Party’s reasonable efforts to avoid or mitigate such event or circumstance. Force Majeure Events include, without limitation, acts of God; natural disasters; epidemics, pandemics, or public health emergencies; war, terrorism, civil unrest, or sabotage; governmental actions, orders, or changes in law; failures, interruptions, or shortages of utilities, telecommunications, or transportation; failures or delays of third-party service providers or vendors; widespread network or platform outages; technical disruptions, cyber incidents, or malware not caused by the affected Party’s breach of its obligations under this Agreement. For the avoidance of doubt, a Force Majeure Event shall excuse the affected Party’s performance and any associated service levels or timelines only to the extent and for the duration such performance is prevented or delayed by the Force Majeure Event, and the Buyer shall have no obligation to pay for Services not performed due to a Force Majeure Event. |
| 1.13 | “Intellectual Property” shall have the meaning set forth in the Purchase Agreement. |
| 1.14 | “Laws” means all applicable laws, rules, and regulations in the jurisdictions where the Services are performed; for cross-border data, the Parties will follow the DPA and agreed transfer mechanics. |
| 1.15 | “OTD” means Order-to-Delivery services. |
| 1.16 | “OTC” means Order-to-Cash services. |
| 1.17 | “Operating Budget” means the budget for CGM Direct Operating Costs attached as Exhibit 1.17, including any line-item overages within the Buyer Approver Overage or other exceptions pre-approved in writing by Buyer. |
| 1.18 | “Performance Standard” [***]. |
| 1.19 | “Selected Territories” means the United States, Germany, Italy, Spain and Sweden. |
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2.1Transition Services. On the terms and subject to the conditions set forth in this Agreement, and in supporting the transfer, transition (in accordance with the Performance Standard), and subsequent operation, of the Business to and by Buyer pursuant to the terms and conditions set forth in the Purchase Agreement, commencing on the date of the Closing of the Purchase Agreement transactions in the U.S., Ascensia shall provide, independently or through other parties currently providing services to Ascensia, to Buyer all services reasonably necessary to operate the Business in accordance with the Performance Standard, as further described in Schedules A-D described below and attached hereto (collectively, the “Transition Services”). Ascensia shall provide those Transition Services expressly identified on the Schedules (together with any Ancillary Services) to support the operation of the Business in the European Selected Territories during the Term as contemplated by this Agreement in accordance with the Performance Standard. If the Parties mutually agree in writing to add a service inadvertently omitted from the Schedules that is reasonably encompassed within, or necessary to perform, the Transition Services and that is materially consistent with such service as performed as of the Effective Date in connection with the operation of the Business in the European Selected Territories (subject to Ascensia’s resource availability, applicable security, compliance, and policy requirements, and without additional fees, pass-through charges, or incremental costs to Buyer), Ascensia will provide such service as a Transition Service. Any service that constitutes a net-new service not reasonably contemplated by the Schedules shall be subject to mutual agreement of the Parties as to scope and applicable fees, if any. Transition Services shall include: (i) shared services set forth in Schedule A (“Shared Services”); (ii) employee support services set forth in Schedule B (“Employee Services”); (iii) the coverage and support of Ascensia’s BGM sales force as set forth in Schedule C (“BGM Services”); and (iv) tender maintenance and management services as further described in Schedule D (“Tender Management Services”). All Schedules shall be deemed incorporated into this Agreement. Notwithstanding the foregoing, the Parties agree that the Transition Services offered under this Agreement, for the amounts set forth in the schedules and subject to the Fee Cap, shall include provision of the following services in accordance with the Performance Standard: (i) order to cash services (including for 365 product if approved), and (ii) human resource services related to the Employee Services (in each case, with respect to the foregoing clauses (i)-(ii), to the extent offered by Ascensia in connection with the operation of the Business in the European Selected Territories as of the Effective Date. For the avoidance of doubt, the fees for OTC and OTD service line items are fully capped as set forth in the line items of the applicable Schedule, and shall not be subject to increase or adjustment except to the extent Buyer expressly requests in writing a change in the scope or delivery method of such services beyond those contemplated by the Schedules and the transition planned to effect the Purchase Agreement pursuant to Section 2.2. The inclusion of the 365 product or new tenders in such OTC and OTD services shall not constitute a change in scope, provided that Buyer does not request process changes causing a material increase in the cost of such service and that are not inherent in or reasonably required to compliantly perform the services for such inclusion.
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pursuing new tender awards and an update of approvals or tenders for Eversense 365, pursuant to and in accordance with the applicable provisions of Schedule D (other than with respect to (i) declined regulatory services for Eversense 365, or (ii) sales force services with respect to Eversense 365).
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[***] Services rendered prior to the Effective Date in anticipation of this Agreement shall be included on the next monthly invoice. Buyer shall have the right to review supporting documentation for all CGM Direct Operating Costs.
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13
14
[Signature page on next page.]
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IN WITNESS WHEREOF, the Parties have caused this Agreement to be duly executed as of the day and year first above written.
Senseonics, Incorporated
By: /s/ Timothy T. Goodnow, Ph.D.
Name: Timothy T. Goodnow, Ph.D.
Title: President and CEO
---------------------
Ascensia Diabetes Care Holdings AG
(two signatories required)
By:
Name: Koichiro Sato
Title: Chief Executive Officer
Ascensia Diabetes Care Holdings AG
(two signatories required)
By:
Name: Marieke Jansen
[Signature Page to Transition Services Agreement]
IN WITNESS WHEREOF, the Parties have caused this Agreement to be duly executed as of the day and year first above written.
Senseonics, Incorporated
By:
Name:
Title:
---------------------
Ascensia Diabetes Care Holdings AG
(two signatories required)
By: /s/ Koichiro Sato
Name: Koichiro Sato
Title: Chief Executive Officer
Ascensia Diabetes Care Holdings AG
(two signatories required)
By: /s/ Marieke Jansen
Name: Marieke Jansen
[Signature Page to Transition Services Agreement]
SCHEDULE A
Shared Services
[***]
SCHEDULE B
Employee Services
[***]
SCHEDULE C
BGM Sales Force Coverage
[***]
SCHEDULE D
Tender Management Services
[***]
EXHIBIT 10.3
CERTAIN PORTIONS OF THIS EXHIBIT (INDICATED BY [***]) HAVE BEEN EXCLUDED PURSUANT TO ITEM 601(B)(10) OF REGULATION S-K BECAUSE THEY ARE BOTH NOT MATERIAL AND ARE THE TYPE THAT THE COMPANY TREATS AS PRIVATE AND CONFIDENTIAL.
THIS FIRST AMENDMENT TO AMENDED AND RESTATED COLLABORATION AND COMMERCIALIZATION AGREEMENT (this “Amendment”) is entered into as of March 12, 2026 (the “Amendment Effective Date”) by and between Senseonics, Incorporated, a Delaware corporation (“Senseonics”) and Ascensia Diabetes Care Holdings AG (“Ascensia”).
RECITALS
WHEREAS, Senseonics and Ascensia have entered into that certain Amended and Restated Collaboration and Commercialization Agreement, dated December 31, 2025 (the “Agreement”); and
WHEREAS, the parties desire to amend the Agreement as set forth herein.
NOW, THEREFORE, in consideration of the mutual promises and covenants herein and other consideration, the receipt and sufficiency of which is hereby acknowledged, the parties hereby agree as follow:
AGREEMENT
“Tender Agreement” means any agreement with respect to Italy, Spain and/or Sweden, between Ascensia and any local or regional governmental entity or governmental body for the Supply of Products in the Field to a pre-defined user group.
Promotional Materials. Senseonics will be responsible for reviewing and approving key advertising, sales information, literature, and other promotional materials pertaining Products (“Promotional Material”) prior to use or dissemination by Ascensia in the Territories. Senseonics is fully responsible for ensuring all new materials are compliant according to relevant legal, medical, and regulatory standards. Notwithstanding the foregoing, any Promotional Materials that are in use by Ascensia in the Territory as of the Amended Effective Date and have been previously approved by Senseonics (if and to the extent such approval was required under the Prior Agreement) may continue to be used by Ascensia without further review or approval by Senseonics, so long as they remain accurate, compliant with applicable law and consistent with this Agreement.
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4.3 Taxes. Unless otherwise provided on the Purchase Order, in addition to the amounts stated above, Senseonics shall pay costs for all sales, use, value-added or excise taxes, assessments or other charges, including customs duties and similar fees attributable to the sale of the Product. In the event Ascensia pays any such fees, taxes, or charges, Ascensia shall promptly invoice Senseonics for the same pursuant to the Transition Services Agreement, except that duties import are to be included in the COGS per section 4.4 and settled through the corresponding true-up.
4.4 Transition True-up. For the period from [***], or [***], the Parties shall conduct a monthly true-up to account for [***]. For such true-up, the amounts owed to Senseonics under the 100% revenue share shall be reduced to the extent of [***], to the extent that (i) such amounts are actually incurred and paid out in the period and (ii) such amounts are not otherwise attributable to or accounted for under the Transition Services Agreement, including without limitation under Schedule A cost sharing, Schedule B, payments for operating expenses, or otherwise.
[Signature Page Follows]
2
IN WITNESS WHEREOF, the parties confirm and acknowledge the terms of this Agreement. The parties represent and warrant that the persons executing this Amendment have all necessary authority to enter into, and bind the relevant entity, to this Amendment.
|
Senseonics: Senseonics, Incorporated Signature: /s/ Timothy T. Goodnow, Ph.D. Name: Timothy T. Goodnow, Ph.D. Title: President and CEO Date: March 12, 2026 |
Ascensia: Ascensia Diabetes Care Holdings AG Signature: Name: Title: Date: Signature: Name: Title: Date: |
[Signature Page to First Amendment to Amended and Restated Collaboration and Commercialization Agreement]
IN WITNESS WHEREOF, the parties confirm and acknowledge the terms of this Agreement. The parties represent and warrant that the persons executing this Amendment have all necessary authority to enter into, and bind the relevant entity, to this Amendment.
|
Senseonics: Senseonics, Incorporated Signature: Name: Title: Date: |
Ascensia: Ascensia Diabetes Care Holdings AG Signature: /s/ Koichiro Sato Name: Koichiro Sato Title: Chief Executive Officer Date: 3/11/2026 Signature: /s/ Marieke Jansen Name: Marieke Jansen Title: General Counsel Date: 3/11/2026 |
[Signature Page to First Amendment to Amended and Restated Collaboration and Commercialization Agreement]
EXHIBIT 31.1
CERTIFICATION OF PRINCIPAL EXECUTIVE OFFICER
PURSUANT TO SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002
I, Timothy T. Goodnow, Ph.D., certify that:
1. |
I have reviewed this quarterly report on Form 10-Q of Senseonics Holdings, Inc. (the “registrant”); |
2. |
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
3. |
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; |
4. |
The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
(a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;
(b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;
(c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and
(d) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5. |
The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): |
(a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
(b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.
Date: May 7, 2026
|
|
|
/s/ Timothy T. Goodnow, Ph.D. |
|
Timothy T. Goodnow, Ph.D. |
|
President & Chief Executive Officer |
|
(principal executive officer) |
EXHIBIT 31.2
CERTIFICATION OF PRINCIPAL FINANCIAL OFFICER
PURSUANT TO SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002
I, Rick Sullivan, certify that:
1. |
I have reviewed this quarterly report on Form 10-Q of Senseonics Holdings, Inc. (the “registrant”); |
2. |
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
3. |
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; |
4. |
The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
(a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;
(b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;
(c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and
(d) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and
5. |
The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): |
(a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
(b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.
Date: May 7, 2026
|
|
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/s/ Rick Sullivan |
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Rick Sullivan |
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Chief Financial Officer |
|
(principal financial officer) |
EXHIBIT 32.1
CERTIFICATIONS OF
PRINCIPAL EXECUTIVE OFFICER AND PRINCIPAL FINANCIAL OFFICER
PURSUANT TO 18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
Pursuant to the requirement set forth in Rule 13a-14(b) of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), and Section 1350 of Chapter 63 of Title 18 of the United States Code (18 U.S.C. §1350), Timothy T. Goodnow, Ph.D., President and Chief Executive Officer of Senseonics Holdings, Inc. (the “Company”), and Rick Sullivan, Chief Financial Officer of the Company, each hereby certifies that, to the best of his knowledge:
1. |
The Company’s Quarterly Report on Form 10-Q for the quarter ended March 31, 2026 (the “Quarterly Report”), to which this Certification is attached as Exhibit 32.1, fully complies with the requirements of Section 13(a) or Section 15(d) of the Exchange Act, and |
2. |
The information contained in the Quarterly Report fairly presents, in all material respects, the financial condition and results of operations of the Company. |
In Witness Whereof, the undersigned have set their hands hereto as of the 7th day of May 2026.
/s/ Timothy T. Goodnow, Ph.D. |
|
/s/ Rick Sullivan |
Timothy T. Goodnow, Ph.D. |
|
Rick Sullivan |
President & Chief Executive Officer |
|
Chief Financial Officer |
(principal executive officer) |
|
(principal financial officer) |
*This certification accompanies the Form 10-Q to which it relates, is not deemed filed with the Securities and Exchange Commission and is not to be incorporated by reference into any filing of the Company under the Securities Act of 1933, as amended, or the Exchange Act (whether made before or after the date of the Form 10-Q), irrespective of any general incorporation language contained in such filing.