| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 2.06M | 1.63M | 1.07M | 1.21M | 1.18M | 1.04M |
| Gross Profit | 873.85K | 1.08M | 691.90K | 764.28K | 809.30K | 731.38K |
| EBITDA | -17.01M | -16.33M | -13.17M | -10.49M | -6.55M | -5.80M |
| Net Income | -19.80M | -18.82M | -14.25M | -11.39M | -7.54M | -6.91M |
Balance Sheet | ||||||
| Total Assets | 16.29M | 12.45M | 27.76M | 16.90M | 28.58M | 7.61M |
| Cash, Cash Equivalents and Short-Term Investments | 4.57M | 3.45M | 21.72M | 12.96M | 24.78M | 3.32M |
| Total Debt | 8.43M | 7.44M | 6.70M | 543.72K | 990.21K | 2.06M |
| Total Liabilities | 11.73M | 10.14M | 9.40M | 1.65M | 2.24M | 4.08M |
| Stockholders Equity | 4.56M | 2.30M | 18.35M | 15.24M | 26.33M | 3.53M |
Cash Flow | ||||||
| Free Cash Flow | -20.08M | -20.21M | -11.42M | -11.14M | -8.24M | -4.96M |
| Operating Cash Flow | -19.58M | -19.44M | -11.28M | -10.73M | -7.93M | -4.93M |
| Investing Cash Flow | -544.00K | -847.76K | -143.92K | -407.48K | -306.87K | 968.32K |
| Financing Cash Flow | 17.08M | 2.03M | 20.18M | -681.64K | 29.70M | 871.65K |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
58 Neutral | $7.02M | 40.95 | 5.90% | ― | -4.99% | -19.10% | |
52 Neutral | $32.63M | -4.94 | -57.98% | ― | 13.67% | -37.01% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
49 Neutral | $46.54M | -1.11 | -376.23% | ― | 63.53% | 12.49% | |
46 Neutral | $24.55M | -3.68 | -8.05% | ― | -0.95% | 58.17% | |
43 Neutral | $16.84M | -4.12 | -58.34% | ― | 73.38% | 34.87% | |
41 Neutral | $24.27M | -3.52 | -136.47% | ― | 0.59% | -39.76% |
On December 18, 2025, Femasys Inc. reported that it had received 510(k) clearance from the U.S. Food and Drug Administration for its FemVue Controlled diagnostic device, a next-generation solution for controlled contrast delivery during ultrasound imaging to evaluate fallopian tube status. The device combines features of the company’s original FemVue and FemChec technologies into a single FDA-cleared platform, supporting multiple clinical uses such as confirming tubal patency before FemaSeed procedures and is intended to simplify care delivery, enhance workflow efficiency in clinical practice, and streamline manufacturing as Femasys expands its integrated fertility and women’s health product portfolio.
On November 6, 2025, Femasys Inc. announced a significant initial order valued at approximately $500,000 USD for the commercial launch of FemBloc Permanent Birth Control in France and the Benelux region through its partnership with Kebomed. This order marks continued progress in expanding FemBloc’s presence across key European markets, reflecting growing international momentum for this innovative, non-surgical permanent contraceptive solution. FemBloc, a first-of-its-kind non-surgical solution for permanent birth control, addresses a significant unmet need in women’s reproductive health by providing a safer, more convenient, and affordable option compared to surgical sterilization.
Femasys Inc. announced on November 3, 2025, that it has entered into a Securities Purchase Agreement with accredited investors to raise $12 million through a private placement of senior secured convertible notes and warrants. The proceeds will be used to repay existing debt and for general corporate purposes, with company insiders participating in the investment. The agreement grants the lead lender a board nomination right and includes customary covenants and restrictions.
On November 3, 2025, Femasys Inc. announced it has received FDA approval to advance the final phase of the FemBloc trial, a non-surgical permanent birth control method, marking a significant step towards potential U.S. market entry. Additionally, Femasys secured $12 million in financing, with potential to reach $58 million, which will be used to refinance existing debt and support the commercialization of its fertility and birth control portfolio, reflecting strong investor confidence in the company’s mission to transform women’s health.
On May 19, 2025, Femasys Inc. received a notice from Nasdaq indicating that its common stock had fallen below the minimum market value requirement for continued listing. However, after a recent offering and warrant exercises, the company reported a pro forma stockholders’ equity of approximately $5.2 million as of October 15, 2025, meeting Nasdaq’s minimum requirement. Nasdaq will continue to monitor Femasys’ compliance, and failure to maintain these standards could result in delisting.
On October 13, 2025, Daniel Currie, Chief Operating Officer of Femasys Inc., announced his retirement effective December 15, 2025, after over 20 years with the company. His departure is due to personal health reasons and a desire to focus on family. The company has entered into a Separation Agreement with Currie, ensuring the vesting of unvested stock options and continuation of health benefits through 2026. The Board of Directors expressed their gratitude for his leadership and service.