Medical Device Manufacturer · US , Princeton , NJ

Orthovita Co. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1995

Total

Cleared

Denied

Orthovita Co. has 3 FDA 510(k) cleared medical devices. Based in Princeton, US.

Historical record: 3 cleared submissions from 1995 to 2000. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Orthovita Co.

3 devices

1-3 of 3