Ustomed Instrumente Ulrich Storz GmbH & Co. KG
GermanyFDA applicant, unverified
- Devices
- 1
What Ustomed Instrumente Ulrich Storz GmbH & Co. KG makes
Ustomed Instrumente Ulrich Storz GmbH & Co. KG manufactures bone fixation and augmentation systems, including intramedullary pins (PINs) for orthopedic applications.
These devices are classified as Class II under regulatory frameworks and are listed via FDA 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ustomed Instrumente Ulrich Storz GmbH & Co. KG have in the registry?
The registry currently lists 1 device for Ustomed Instrumente Ulrich Storz GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ustomed Instrumente Ulrich Storz GmbH & Co. KG's devices?
Among its 1 most recently registered device, Ustomed Instrumente Ulrich Storz GmbH & Co. KG has devices listed in FDA 510(k) (1 device).
What risk classes do Ustomed Instrumente Ulrich Storz GmbH & Co. KG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ustomed Instrumente Ulrich Storz GmbH & Co. KG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ustomed Instrumente Ulrich Storz GmbH & Co. KG in the registry?
The most recently registered devices listed for Ustomed Instrumente Ulrich Storz GmbH & Co. KG include USTOMED Bone Fixation/Bone Augmentation Systems - PIN.