Artivion's biggest risks in the FY2024 10-K
- Artivion relies heavily on tissue preservation services, BioGlue, aortic stent grafts, and On-X products for its revenues.
- Operations face strict regulatory scrutiny regarding medical devices, human tissues, and sterilization processes like EtO.
- Growth depends on ongoing clinical studies, regulatory approvals, and international expansion.
The risks most specific to Artivion
- Business and Economic Risks
We are significantly dependent on our revenues from tissue preservation services and are subject to a variety of risks affecting them
We depend significantly on revenues from tissue preservation services and rely on third parties to foster public tissue donation.
- Business and Economic Risks
We are significantly dependent on our revenues from BioGlue and are subject to a variety of related risks
Any adverse impact on our BioGlue products or delays in non-US commercialization approvals would materially harm our financial results.
- Business and Economic Risks
We are significantly dependent on our revenues from aortic stent grafts and are subject to a variety of related risks
Our aortic stent graft revenues depend on our ability to innovate and respond to enhanced regulatory requirements and enforcement.
- Business and Economic Risks
We are significantly dependent on our revenues from On-X products and are subject to a variety of related risks
Our On-X product revenues depend on taking market share via the FDA's approved lower INR indication for the aortic heart valve.
- Operational Risks
We are dependent on single and sole-source suppliers and single facilities
We rely on single- and sole-source suppliers and single facilities for certain materials, supplies, services, and products.
- Legal, Quality, and Regulatory Risks
Reclassification by the FDA of CryoValve SG pulmonary heart valve (“CryoValve SGPV”) may make it commercially infeasible to continue processing the CryoValve SGPV
Proposed FDA reclassification of minimally manipulated allograft heart valves to Class III could make processing the CryoValve SGPV commercially infeasible.
- Legal, Quality, and Regulatory Risks
Increased environmental regulations and private litigation activity relating to processes and materials used in our industry could have a material, adverse impact on us
We and our third-party suppliers use ethylene oxide for sterilization, exposing us to increased environmental regulations and private litigation.
- Legal, Quality, and Regulatory Risks
In addition, any litigation, regulatory enforcement, or government regulation regarding the use of EtO could result in financial, legal, business, and reputational harm to us
PFAS used in medical devices and packaging face increasing regulations and potential bans by the EPA and numerous states.
All 33 risk factors
Headings as the filing states them, in filing order.
Business and Economic Risks
- 01We are subject to a variety of risks due to our international operations and continued global expansion
- 02We operate in highly competitive market segments, face competition from large, well-established medical device companies and tissue service providers with greater resources and we may not be able to compete effectively
- 03We are significantly dependent on our revenues from tissue preservation services and are subject to a variety of risks affecting them
- 04We are significantly dependent on our revenues from BioGlue and are subject to a variety of related risks
- 05We are significantly dependent on our revenues from aortic stent grafts and are subject to a variety of related risks
- 06We are significantly dependent on our revenues from On-X products and are subject to a variety of related risks
- 07Continued fluctuation of foreign currencies relative to the US Dollar could materially, adversely affect our business
- 08Some of our products and technologies are subject to significant intellectual property risks and uncertainty
- 09Public health crises have, may continue to have, and could have a material, adverse impact on us
Operational Risks
- 10We are heavily dependent on our suppliers and contract manufacturers to provide quality products
- 11We are dependent on single and sole-source suppliers and single facilities
- 12We are dependent on our specialized workforce
- 13We continue to evaluate expansion through acquisitions of, or licenses with, investments in, and distribution arrangements with, other companies or technologies, which may carry significant risks
- 14Our charges resulting from acquisitions, divestitures, partnerships, and other business development activities may materially, adversely affect the market value of our common stock
- 15We may not realize all the anticipated benefits of our business development activities
- 16Significant disruptions of information technology systems or breaches of information security systems could adversely affect our business
- 17Our business could be impacted by environmental, social, and governance matters
Legal, Quality, and Regulatory Risks
- 18Our products and tissues are highly regulated and subject to significant quality and regulatory risks
- 19Reclassification by the FDA of CryoValve SG pulmonary heart valve (“CryoValve SGPV”) may make it commercially infeasible to continue processing the CryoValve SGPV
- 20We may not be successful in obtaining clinical results or regulatory clearances/approvals for new and existing products and services, and our approved products and services may not achieve market acceptance
- 21Each of our trials, studies, and approvals is subject to the risks outlined herein
- 22Increased environmental regulations and private litigation activity relating to processes and materials used in our industry could have a material, adverse impact on us
- 23In addition, any litigation, regulatory enforcement, or government regulation regarding the use of EtO could result in financial, legal, business, and reputational harm to us
- 24We may be subject to fines, penalties, and other sanctions if we are deemed to be promoting the use of our products for unapproved, or off-label, uses
- 25We are subject to various US and international bribery, anti-kickback, false claims, privacy, transparency, and similar laws, any breach of which could cause a material, adverse effect on our business, financial condition, and profitability
- 26United States policy changes may have a material, adverse effect on us
- 27As a medical device manufacturer and tissue services provider we are exposed to risk of product liability claims and our existing insurance coverage may be insufficient, or we may be unable to obtain insurance in the future, to cover any resulting liability
- 28Failure to comply with data privacy and security laws could have a material adverse effect on our business
Risks Relating to Our Indebtedness
- 29The agreements governing our indebtedness contain restrictions that limit our flexibility in operating our business
- 30Our indebtedness could adversely affect our ability to raise additional capital to fund operations and execute our strategic plan, and limit our ability to react to changes in the economy or our industry
Risks Relating to Ownership of our Common Stock
- 31Our business could be negatively impacted as a result of stockholder activism
- 32We do not anticipate paying any dividends on our common stock for the foreseeable future
- 33Provisions of Delaware law and anti-takeover provisions in our organizational documents may discourage or prevent a change of control, even if an acquisition would be beneficial to stockholders, which could affect our share price adversely and prevent attempts by stockholders to remove current management
Other Artivion 10-Ks
- FY2025 10-K risk factors34 risks1 new4 reworded
A new U.S. healthcare and tax law creates uncertainty around corporate taxes, deductions, and healthcare programs.
Filed Feb 18, 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.