Coroventis Research AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Coroventis Research AB - FDA 510(k) Cleared Devices
Recent clearances: CoroFlow Cardiovascular System, CoroFlow Cardiovascular System
2
Total
2
Cleared
0
Denied
Coroventis Research AB has 2 FDA 510(k) cleared medical devices. Based in Uppsala, SE.
Latest FDA clearance: Oct 2025. Active since 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Coroventis Research AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Coroventis Research AB
2 devices