FDA approves first acellular tissue engineered vessel to treat vascular trauma in extremities

FDA

20 December 2024 - The US FDA approved Symvess, the first acellular tissue engineered vessel indicated for use in adults as a vascular conduit for extremity arterial injury when urgent revascularisation is needed to avoid imminent limb loss, and autologous vein graft is not feasible.

Symvess is a sterile, acellular tissue engineered vessel composed of human extracellular matrix proteins typically found in human blood vessels.

Read FDA press release

Michael Wonder

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Michael Wonder

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Outcome , US , Cellular therapy