On February 26, 2025, Humacyte, Inc. announced the commercial launch of Symvess (acellular tissue engineered vessel-tyod) for use in adults as a vascular conduit for extremity arterial injury. This follows the full FDA approval of Symvess on December 19, 2024, and the FDA's authorization for commercial shipments.
The company reported positive responses from surgeons and trauma centers, with 21 hospitals already initiating the Value Analysis Committee (VAC) approval process. Two hospitals have completed their review and approved the purchase of Symvess, with others planning purchases while the VAC process is underway.
Symvess offers an off-the-shelf solution for urgent arterial repair, eliminating the need for autologous vein grafts and potentially improving patient outcomes in limb-threatening situations. This launch signifies a new era in vascular surgery and a key growth phase for Humacyte.
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