Intervene is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intervene - FDA 510(k) Cleared Devices
Recent clearances: Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018, FG019, FG020)
1
Total
1
Cleared
0
Denied
Intervene has 1 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Intervene Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mark Smutka as regulatory consultant.
FDA 510(k) Regulatory Record - Intervene
1 devices