Baumer, S.A is one of 50 FDA 510(k) medical device manufacturers from Brazil in the dataset, ranked by real submission volume.
Baumer, S.A - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
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