Dufner Instrumente GmbH is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Dufner Instrumente GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Dufner Instrumente GmbH has 1 FDA 510(k) cleared medical devices. Based in Amsterdam, Nh, NL.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dufner Instrumente GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dufner Instrumente GmbH
1 devices