Avantec Vascular Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Avantec Vascular Corporation - FDA 510(k) Cleared Devices
Recent clearances: Sangria™ Thrombectomy System
2
Total
2
Cleared
0
Denied
Avantec Vascular Corporation has 2 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Latest FDA clearance: Jan 2026. Active since 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Avantec Vascular Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Avantec Vascular Corporation
2 devices