Claronav is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Claronav - FDA 510(k) Cleared Devices
Recent clearances: Navient Image Guided Navigation System (ENT) (955-NC-NC), Navient Image Guide Navigation System (955-NC-NC), Cranial
2
Total
2
Cleared
0
Denied
Claronav has 2 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Claronav Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Claronav
2 devices