Itena Clinical - FDA 510(k) Cleared Devices

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.

510(k) submissions have been managed by Lok North America, Inc. as regulatory consultant.