Microvention is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microvention - FDA 510(k) Cleared Devices
Recent clearances: MV Flow Aspiration Pump (MVFLOWPMP01)
1
Total
1
Cleared
0
Denied
Microvention has 1 FDA 510(k) cleared medical devices. Based in Aliso Veijo, US.
Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Microvention Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Microvention
1 devices