Medical Device Manufacturer · CA , Laval

Itena Clinical - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2013

Total

Cleared

Denied

Itena Clinical has 8 FDA 510(k) cleared medical devices. Based in Laval, CA.

Historical record: 8 cleared submissions from 2013 to 2017. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Itena Clinical Filter by specialty or product code using the sidebar.

Itena Clinical is one of 209 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Itena Clinical

8 devices

1-8 of 8