Conavi Medical, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Conavi Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Novasight Hybrid System, Novasight Hybrid System
3
Total
3
Cleared
0
Denied
Conavi Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Latest FDA clearance: Apr 2026. Active since 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Conavi Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Avania as regulatory consultant. 1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Conavi Medical, Inc.
3 devices