Stork Instrumente GmbH
Country not established FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Stork Instrumente GmbH makes
Stork Instrumente GmbH manufactures orthopedic fixation devices, including bone wires used for internal stabilization in surgical procedures.
Their portfolio is regulated under FDA 510(k) clearance as Class II medical devices and is listed in the US regulatory registry.
Catalogue
Bone Wire Ref K030665
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Stork Instrumente GmbH Emmingen-Liptingen Baden-Wurttemberg · DE FEI 1000168975
Frequently asked questions
How many devices does Stork Instrumente GmbH have in the registry?
The registry currently lists 1 device for Stork Instrumente GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stork Instrumente GmbH's devices?
Among its 1 most recently registered device, Stork Instrumente GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Stork Instrumente GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stork Instrumente GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stork Instrumente GmbH in the registry?
The most recently registered devices listed for Stork Instrumente GmbH include BONE WIRE.
Which FDA establishments are linked to Stork Instrumente GmbH?
1 FDA establishment is linked to Stork Instrumente GmbH in the registry; they are listed on the company page.