Stork Instrumente GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stork Instrumente GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Stork Instrumente GmbH has 1 FDA 510(k) cleared medical devices. Based in Gurnee, US.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Stork Instrumente GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stork Instrumente GmbH
1 devices