Medical Device Manufacturer · US , Arlington , VA

Les Laboratorires Brothier, S.A. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1990

Total

Cleared

Denied

Les Laboratorires Brothier, S.A. has 5 FDA 510(k) cleared medical devices. Based in Arlington, US.

Historical record: 5 cleared submissions from 1990 to 2004. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Les Laboratorires Brothier, S.A. Filter by specialty or product code using the sidebar.

5 devices

1–5 of 5