Eos-Werke, Gunther GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Eos-Werke, Gunther GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Eos-Werke, Gunther GmbH has 1 FDA 510(k) cleared medical devices. Based in West Germany, DE.
Historical record: 1 cleared submissions from 1984 to 1984. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Eos-Werke, Gunther GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eos-Werke, Gunther GmbH
1 devices