enVVeno Medical's biggest risks in the FY2024 10-K
- enVVeno Medical faces extreme concentration risk relying on only two domestic suppliers for porcine tissue.
- The company relies entirely on its Irvine facility for manufacturing product candidates.
- Regulatory hurdles and capital raising needs dominate the risk profile.
The risks most specific to enVVeno Medical
- Risks Related to Our Business and Strategy
We only utilize a few suppliers for porcine tissue for our product candidates and the loss of a supplier could have an adverse impact on our business
We rely on two domestic third-party vendors to supply porcine tissue for our product candidates.
- Risks Related to Our Business and Strategy
We may be unable to convince hospital facilities to approve the use of our product candidates
Hospital facilities require approval from value analysis committees before surgeons can use our product candidates.
- Risks Related to Our Business and Strategy
If we are unable to produce an adequate supply of our product candidates for use in our current and planned clinical trials or for commercialization because of our limited manufacturing resources or our facility is damaged or becomes inoperable, our regulatory, development and commercialization efforts may be delayed
We currently manufacture our product candidates solely at our facility in Irvine, California.
- Risks Related to Regulatory Approval and Other Governmental Regulations
Our product candidates may be subject to extensive governmental regulation in foreign jurisdictions, such as the EEA, and our failure to comply with applicable requirements could cause our business, results of operations and financial condition to suffer
Our product candidates must comply with Medical Device Regulation to obtain a CE mark for sale in the EEA.
- Risks Related to Regulatory Approval and Other Governmental Regulations
The FDA regulatory approval, clearance and license process is complex, time-consuming and unpredictable
We must submit and the FDA must approve a PMA application before our medical device product candidates may be marketed.
- Risks Related to Regulatory Approval and Other Governmental Regulations
We are required to report certain malfunctions, deaths and serious injuries associated with our products once approved by regulatory bodies, which can result in voluntary corrective actions or agency enforcement actions
We are legally bound to report incidents and malfunctions associated with our products in the EEA.
- Risks Related to Regulatory Approval and Other Governmental Regulations
Any of these changes could require substantial time and cost and could harm our business and our financial results
The EU Medical Device Regulation was implemented following the 2010 PIP scandal involving non-medical grade silicone.
- Risks Related to Ownership of Our Securities
Our failure to meet the continued listing requirements of Nasdaq could result in a de-listing of our Common Stock
We have received deficiency notices in the past regarding Nasdaq continued listing requirements.
All 33 risk factors
Headings as the filing states them, in filing order.
Risks Related to Our Business and Strategy
- 01We have incurred losses since our inception, expect to incur losses in the future and may never achieve or sustain profitability
- 02If we are unable to successfully raise additional capital, our future clinical trials and product development could be limited and our long-term viability may be threatened
- 03We may not be able to acquire additional funds on acceptable terms, or at all. If we are unable to raise adequate funds, we may have to liquidate some or all of our assets or delay, reduce the scope of or eliminate some or all of our development programs
- 04We may never be able to generate sufficient revenue from the commercialization of our product candidates to achieve and maintain profitability
- 05We only utilize a few suppliers for porcine tissue for our product candidates and the loss of a supplier could have an adverse impact on our business
- 06We depend upon third-party suppliers for certain components of our product candidates, making us vulnerable to supply problems and price fluctuations, which could harm our business
- 07If we successfully develop product candidates, we will have to demonstrate the efficacy and financial viability of our products to doctors, hospitals, insurance companies, and other stakeholders
- 08We may be unable to convince hospital facilities to approve the use of our product candidates
- 09We face significant competition and our business prospects will depend on our ability to develop and commercialize our current product candidates and may also depend on our ability to develop additional product candidates
- 10If we are unsuccessful in developing and commercializing additional devices in other areas, our ability to realize our revenue may be impaired
- 11If we are unable to produce an adequate supply of our product candidates for use in our current and planned clinical trials or for commercialization because of our limited manufacturing resources or our facility is damaged or becomes inoperable, our regulatory, development and commercialization efforts may be delayed
- 12Product liability lawsuits against us could cause us to incur substantial liabilities, limit sales of our existing product candidates and limit commercialization of any products that we may develop
- 13The loss of our executive officers or our inability to attract and retain qualified personnel may adversely affect our business, financial conditions and results of operations
- 14Our ability to use our net operating loss carryforwards and certain other tax attributes may be limited
Risks Related to Regulatory Approval and Other Governmental Regulations
- 15Our business and product candidates are subject to extensive governmental regulation and oversight, and our failure to comply with applicable regulatory requirements could harm our business
- 16Our product candidates may be subject to extensive governmental regulation in foreign jurisdictions, such as the EEA, and our failure to comply with applicable requirements could cause our business, results of operations and financial condition to suffer
- 17The FDA regulatory approval, clearance and license process is complex, time-consuming and unpredictable
- 18Even if our product candidates are approved by regulatory authorities, if we fail to comply with ongoing regulatory requirements, or if we experience unanticipated problems with our product candidates, our product candidates could be subject to restrictions or withdrawal from the market
- 19We are required to report certain malfunctions, deaths and serious injuries associated with our products once approved by regulatory bodies, which can result in voluntary corrective actions or agency enforcement actions
- 20Legislative or regulatory reforms in the United States or the EU may make it more difficult and costly for us to obtain regulatory clearances or approvals for product candidates or to manufacture, market or distribute product candidates after clearance or approval is obtained
- 21Any of these changes could require substantial time and cost and could harm our business and our financial results
- 22We are subject to federal, state and foreign healthcare laws and regulations, and a finding of failure to comply with such laws and regulations could have a material and adverse effect on our business
- 23Regulatory healthcare reform measures and other legislative changes may have a material and adverse effect on business, results of operations and financial condition
- 24Our relationships with physician consultants, owners and investors could be subject to additional scrutiny from regulatory enforcement authorities and could subject us to possible administrative, civil or criminal sanctions
Risks Related to Our Intellectual Property
- 25If we are unable to adequately protect our proprietary technology or obtain and maintain issued patents that are sufficient to protect our product candidates, others could compete against us more directly, which could harm our business, financial condition and results of operations
- 26Obtaining and maintaining our patent protection depends on compliance with various procedures, document submission requirements, fee payments and other requirements imposed by governmental patent agencies, and our patent protection could be reduced or eliminated for non-compliance with these requirements
- 27Our success will depend in part on our ability to operate without infringing the intellectual property and proprietary rights of third parties. Our business, product candidates and methods could infringe the patents or other intellectual property rights of third parties
Risks Related to Ownership of Our Securities
- 28The trading price of our securities has been and is likely to continue to be volatile and could be subject to wide fluctuations in response to a variety of factors
- 29We will need to raise additional capital to meet our business requirements in the future, and such capital raising may be costly or difficult to obtain and can be expected to dilute current stockholders’ ownership interests
- 30Future sales or issuances of substantial amounts of our common stock could result in significant dilution
- 31Our failure to meet the continued listing requirements of Nasdaq could result in a de-listing of our Common Stock
- 32Provisions of our charter documents or Delaware law could delay or prevent an acquisition of us, even if the acquisition would be beneficial to our stockholders, which could make it more difficult for you to change management
- 33We do not anticipate paying any cash dividends on our common stock in the foreseeable future and, as such, capital appreciation, if any, of our common stock will be your sole source of gain for the foreseeable future
Other enVVeno Medical 10-Ks
- FY2025 10-K risk factors34 risks1 new4 reworded
The company received an FDA not-approvable letter for the VenoValve PMA application on August 19, 2025. The FDA cited insufficient hemodynamic correlation and surgical safety concerns, highlighting regulatory hurdles.
Filed Mar 26, 2026
About this page
The headings are the filing's own. The one-line readings and the overview are automated and can be wrong: read Item 1A of the 10-K for the exact wording.