Medical Device Manufacturer · FR , Vigneux De Bretagne

Biomatlante - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2003

Total

Cleared

Denied

Biomatlante has 8 FDA 510(k) cleared medical devices. Based in Vigneux De Bretagne, FR.

Historical record: 8 cleared submissions from 2003 to 2010. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Biomatlante

8 devices

1-8 of 8