Avantec Vascular Corporation is one of 16283 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, Captus Vascular Retrieval 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.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Avantec Vascular Corporation
2 devices