Zeppelin GmbH
GermanyFDA 510(k) applicant, unverified
- Devices
- 2
What Zeppelin GmbH makes
Zeppelin GmbH manufactures surgical instruments for spinal and neurosurgical procedures, including a laminectomy rongeur for bone removal and the Mainz head fixation device by Pernetzky for cranial stabilization during surgery.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II medical devices and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Laminectomy Rongeur Ref K901372
510(k) 510(k)Mainz Head Fixation By Perneczky Ref K901393
510(k) 510(k)
Frequently asked questions
How many devices does Zeppelin GmbH have in the registry?
The registry currently lists 2 devices for Zeppelin GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zeppelin GmbH's devices?
Among its 2 most recently registered devices, Zeppelin GmbH has devices listed in FDA 510(k) (2 devices).
What risk classes do Zeppelin GmbH's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Zeppelin GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Zeppelin GmbH in the registry?
The most recently registered devices listed for Zeppelin GmbH include LAMINECTOMY RONGEUR and MAINZ HEAD FIXATION BY PERNECZKY.