Medical Device Manufacturer · CA , Toronto

Claronav, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2016

Total

Cleared

Denied

Claronav, Inc. has 4 FDA 510(k) cleared medical devices. Based in Toronto, CA.

Latest FDA clearance: Jul 2024. Active since 2016. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Claronav, Inc. Filter by specialty or product code using the sidebar.

Claronav, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Claronav, Inc.

4 devices

1-4 of 4