Medical Device Manufacturer · BR , Mogi Mirim, Sao Paulo

Baumer, S.A - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2000

Total

Cleared

Denied

Baumer, S.A has 4 FDA 510(k) cleared medical devices. Based in Mogi Mirim, Sao Paulo, BR.

Historical record: 4 cleared submissions from 2000 to 2001. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Baumer, S.A

4 devices

1-4 of 4