Medical Device Manufacturer · US , Industry , CA

Dentamerica - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1996

Total

Cleared

Denied

Dentamerica has 4 FDA 510(k) cleared medical devices. Based in Industry, US.

Historical record: 4 cleared submissions from 1996 to 2010. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Dentamerica

4 devices

1-4 of 4