Stuckenbrock Medizintechnik GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stuckenbrock Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: IXOS Radius Plate System, HBS2 Headless Bone Screw
3
Total
3
Cleared
0
Denied
Stuckenbrock Medizintechnik GmbH has 3 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 3 cleared submissions from 2004 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Stuckenbrock Medizintechnik GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stuckenbrock Medizintechnik GmbH
3 devices