Full Press Release Details
Femasys Announces Second Quarter Financial Results for 2025
-- Continued Progress on Regulatory Approvals and Global Commercialization of Fertility Portfolio --
ATLANTA, August 8, 2025 -- Femasys Inc. (NASDAQ: FEMY), a leading biomedical innovator making fertility and non-surgical permanent birth control more accessible and cost-effective to women worldwide, announced its financial results for the
second quarter of 2025.
Corporate Highlights from 2Q 2025 to date
"Our second quarter marked several significant milestones for Femasys as we continue to secure key regulatory approvals, add partners, and strengthen our team to accelerate
the commercialization of our innovative fertility portfolio across the globe," said Kathy Lee-Sepsick, Chief Executive Officer and Founder of Femasys. "European approval of the entire FemBloc System announced in June marks the first global regulatory
endorsement of our groundbreaking non-surgical permanent birth control solution. FemBloc is commercially available through strategic distribution partnerships in select countries in Europe beginning in Spain, who placed their initial order, and we
will seek additional country approvals while continuing to enroll participants in our FDA IDE-approved late-stage pivotal trial for U.S. approval.
"Regulatory approvals for FemaSeed in Australia and New Zealand announced in July also provide us with the opportunity to pursue meaningful commercial opportunities as we
continue to grow revenue and broaden our global footprint. Our new partnership with Carolinas Fertility Institute will help us reach and support more patients earlier in their fertility journey. We look forward to building upon this momentum as we
work towards transforming the fertility sector not only for patients, but also providers."
Financial Results for Quarter Ended June 30, 2025
Financial Results for Six Months Ended June 30, 2025
For more information, please refer to the Company's Form 10-Q filed August 8, 2025, which can be accessed on the SEC
Condensed Balance Sheets
| Assets | June 30, 2025 | December 31, 2024 | ||||||
| Current assets: | ||||||||
| Cash and cash equivalents | $ | 3,218,067 | 3,451,761 | |||||
| Accounts receivable, net | 254,584 | 488,373 | ||||||
| Inventory | 5,232,738 | 3,046,323 | ||||||
| Prepaid and other current assets | 1,045,591 | 1,035,993 | ||||||
| Total current assets | 9,750,980 | 8,022,450 | ||||||
| Property and equipment, at cost: | ||||||||
| Leasehold improvements | 1,238,886 | 1,238,886 | ||||||
| Office equipment | 68,530 | 60,921 | ||||||
| Furniture and fixtures | 417,876 | 417,876 | ||||||
| Machinery and equipment | 3,211,109 | 2,856,740 | ||||||
| Construction in progress | 548,426 | 762,445 | ||||||
| 5,484,827 | 5,336,868 | |||||||
| Less accumulated depreciation | (3,884,964 | ) | (3,740,769 | ) | ||||
| Net property and equipment | 1,599,863 | 1,596,099 | ||||||
| Long-term assets: | ||||||||
| Lease right-of-use assets, net | 1,544,724 | 1,805,543 | ||||||
| Intangible assets, net of accumulated amortization | 55,638 | 65,918 | ||||||
| Other long-term assets | 829,204 | 954,992 | ||||||
| Total long-term assets | 2,429,566 | 2,826,453 | ||||||
| Total assets | $ | 13,780,409 | 12,445,002 |
Condensed Balance Sheets
| Liabilities and Stockholders' Equity | June 30, 2025 | December 31, 2024 | ||||||
| Current liabilities: | ||||||||
| Accounts payable | $ | 3,263,584 | 1,419,044 | |||||
| Accrued expenses | 1,052,752 | 1,151,049 | ||||||
| Convertible notes payable, net (including related parties) | 6,080,813 | 5,406,228 | ||||||
| Clinical holdback - current portion | 63,990 | 88,581 | ||||||
| Lease liabilities - current portion | 502,468 | 517,967 | ||||||
| Total current liabilities | 10,963,607 | 8,582,869 | ||||||
| Long-term liabilities: | ||||||||
| Clinical holdback - long-term portion | 40,348 | 39,611 | ||||||
| Lease liabilities - long-term portion | 1,269,019 | 1,518,100 | ||||||
| Total long-term liabilities | 1,309,367 | 1,557,711 | ||||||
| Total liabilities | 12,272,974 | 10,140,580 | ||||||
| Commitments and contingencies | ||||||||
| Stockholders' equity: | ||||||||
| Common stock, $.001 par, 200,000,000 authorized, 32,692,630 shares issued and 32,575,407 outstanding as of June 30, 2025; and 23,473,149 shares issued and 23,355,926 outstanding as of December 31, 2024 | 32,693 | 23,473 | ||||||
| Treasury stock, 117,223 common shares | (60,000 | ) | (60,000 | ) | ||||
| Warrants | 1,821,744 | 1,860,008 | ||||||
| Additional paid-in-capital | 137,394,016 | 127,679,198 | ||||||
| Accumulated deficit | (137,681,018 | ) | (127,198,257 | ) | ||||
| Total stockholders' equity | 1,507,435 | 2,304,422 | ||||||
| Total liabilities and stockholders' equity | $ | 13,780,409 | 12,445,002 |
Condensed Statements of Comprehensive Loss
| Three Months Ended June 30, | Six Months Ended June 30, | |||||||||||||||
| 2025 | 2024 | 2025 | 2024 | |||||||||||||
| Sales | $ | 409,268 | 221,484 | 750,532 | 492,624 | |||||||||||
| Cost of sales (excluding depreciation expense) | 158,171 | 73,125 | 275,437 | 161,657 | ||||||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | 1,414,429 | 1,975,875 | 4,382,901 | 3,746,606 | ||||||||||||
| Sales and marketing | 984,977 | 975,190 | 1,893,544 | 1,275,677 | ||||||||||||
| General and administrative | 1,616,972 | 1,611,817 | 3,339,685 | 3,114,621 | ||||||||||||
| Depreciation and amortization | 86,285 | 67,628 | 171,138 | 138,856 | ||||||||||||
| Total operating expenses | 4,102,663 | 4,630,510 | 9,787,268 | 8,275,760 | ||||||||||||
| Loss from operations | (3,851,566 | ) | (4,482,151 | ) | (9,312,173 | ) | (7,944,793 | ) | ||||||||
| Other (expense) income: | ||||||||||||||||
| Interest income | 17,144 | 184,138 | 36,173 | 408,822 | ||||||||||||
| Interest expense | (491,500 | ) | (388,311 | ) | (950,949 | ) | (749,863 | ) | ||||||||
| Other expense | (260,000 | ) | - | (260,000 | ) | - | ||||||||||
| Total other expense, net | (734,356 | ) | (204,173 | ) | (1,174,776 | ) | (341,041 | ) | ||||||||
| Loss before income taxes | (4,585,922 | ) | (4,686,324 | ) | (10,486,949 | ) | (8,285,834 | ) | ||||||||
| Income tax benefit | - | (1,750 | ) | (4,188 | ) | (1,750 | ) | |||||||||
| Net loss | $ | (4,585,922 | ) | (4,684,574 | ) | (10,482,761 | ) | (8,284,084 | ) | |||||||
| Net loss attributable to common stockholders, basic and diluted | $ | (4,585,922 | ) | (4,684,574 | ) | (10,482,761 | ) | (8,284,084 | ) | |||||||
| Net loss per share attributable to common stockholders, basic and diluted | $ | (0.16 | ) | (0.21 | ) | (0.39 | ) | (0.38 | ) | |||||||
| Weighted-average shares used in computing net loss per share attributable to common stockholders, basic and diluted | 28,880,704 | 22,215,516 | 27,025,277 | 21,995,436 |
Femasys is a leading biomedical innovator focused on making fertility and non-surgical permanent birth control more accessible and cost-effective for women worldwide
through its broad, patent-protected portfolio of novel, in-office therapeutic and diagnostic products. As a U.S. manufacturer with global regulatory approvals, Femasys is actively commercializing its lead product innovations in the U.S. and key
international markets. Femasys' fertility portfolio includes FemaSeed Intratubal Insemination, a groundbreaking first-step infertility treatment and FemVue , a companion diagnostic for fallopian tube assessment. Published
clinical trial data demonstrates FemaSeed is over twice as effective as traditional IUI, with a comparable safety profile, and high patient and practitioner satisfaction.1
FemBloc permanent birth control is the first and only non-surgical, in-office alternative to centuries-old surgical sterilization that received full regulatory
approval in Europe in June of 2025. Commercialization of this highly cost-effective, convenient and significantly safer approach will be completed through strategic partnerships in select European countries. Alongside FemBloc, the FemChec ,
diagnostic product provides an ultrasound-based test to confirm procedural success. Published data from initial clinical trials demonstrated compelling effectiveness, five-year safety, and high patient and practitioner satisfaction.2 For
U.S. FDA approval, enrollment in the FINALE pivotal trial (NCT05977751) is on-going.
Facebook and LinkedIn.
1Liu, J. H., Glassner, M., Gracia, C. R., Johnstone, E. B., Schnell, V. L., Thomas, M. A., L. Morrison, Lee-Sepsick, K. (2024). FemaSeed Directional Intratubal
Artificial Insemination for Couples with Male-Factor or Unexplained Infertility Associated with Low Male Sperm Count. J Gynecol Reprod Med, 8(2), 01-12. doi:
10.33140/JGRM.08.02.08.
2Liu, J. H., Blumenthal, P. D., Casta o, P. M., Chudnoff, S.
C., Gawron, L. M., Johnstone, E. B., Lee-Sepsick, K. (2025). FemBloc Non-Surgical Permanent Contraception for Occlusion of the Fallopian Tubes. J Gynecol Reprod Med, 9(1),
01-12. doi: 10.33140/JGRM.09.01.05.
Forward-Looking Statements
This press release contains forward-looking statements that are subject to substantial risks and uncertainties. Forward-looking statements can be
identified by terms such as "may," "will," "should," "expect," "plan," "anticipate," "could," "pending," "intend," "believe," "suggests," "potential," "hope," or "continue" or the negative of these terms or other similar expressions, although not all
forward-looking statements contain these words. Forward-looking statements are based on our current expectations and are subject to inherent uncertainties, risks and assumptions, many of which are beyond our control, difficult to predict and could
cause actual results to differ materially from what we expect. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. Factors that could cause actual results to differ include,
among others: our ability to obtain regulatory approvals for our FemBloc product candidate; develop and advance our current FemBloc product candidate and successfully enroll and complete the clinical trial; the ability of our clinical trial to
demonstrate safety and effectiveness of our product candidate and other positive results; estimates regarding the total addressable market for our products and product candidate; our ability to commercialize our products and product candidate, our
ability to establish, maintain, grow or increase sales and revenues, or the effect of delays in commercializing our products, including FemaSeed; our business model and strategic plans for our products, technologies and business, including our
implementation thereof; and those other risks and uncertainties described in the section titled "Risk Factors" in our Annual Report on Form 10-K for the year ended December 31, 2024, and other reports as filed with the SEC. Forward-looking statements
contained in this press release are made as of this date, and Femasys undertakes no duty to update such information except as required under applicable law.