Biomet Merck GmbH is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Biomet Merck GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Biomet Merck GmbH has 1 FDA 510(k) cleared medical devices. Based in Ried Bei Kerzers, CH.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biomet Merck GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biomet Merck GmbH
1 devices