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.

Les Laboratorires Brothier, S.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Les Laboratorires Brothier, S.A.

5 devices

1-5 of 5