USTOMED Bone Fixation/Bone Augmentation Systems - PIN
Jun 2025
270d
Ustomed Instrumente Ulrich Storz GmbH & Co. KG
1
Total
1
Cleared
0
Denied
Ustomed Instrumente Ulrich Storz GmbH & Co. KG — FDA 510(k) Submissions
Ustomed Instrumente Ulrich Storz GmbH & Co. KG has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Screw, Fixation, Intraosseous . Use the specialty filter in the sidebar to narrow results.
1 devices