Sangria™ Thrombectomy System

Sangria™ Thrombectomy System is an FDA 510(k)-cleared medical device (K251207) manufactured by Avantec Vascular Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 6, 2026. Regulation: 8.