Market AdoptionHospital reviews of Symvess already underway, with 21 hospitals having initiated their review and approval process, indicating a strong start for the product's launch.
Product LaunchHumacyte has officially launched SYMVESS, its acellular tissue-engineered vessel (ATEV), in the vascular trauma indication, marking a significant milestone for the company's first FDA-approved commercial indication.
Regulatory ApprovalThe FDA granted Humacyte full approval for Symvess use in adults as a vascular conduit for extremity arterial injury, highlighting regulatory confidence in the product.