Von Zeppelin GmbH
GermanyFDA 510(k) applicant, unverified
- Devices
- 5
Catalogue
Perneczky Aneurysm Clip Ref K901312
510(k) 510(k)Instruments For Neurological Surgery Ref K901313
510(k) 510(k)Perneczky Clip Applier/Remover Ref K954658
510(k) 510(k)Zmm 2000 Zeppelin Millennium Motordrill System Ref K013091
510(k) 510(k)Intervertebral Disc Rongeur Ref K903151
510(k) 510(k)
Frequently asked questions
How many devices does Von Zeppelin GmbH have in the registry?
The registry currently lists 5 devices for Von Zeppelin GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Von Zeppelin GmbH's devices?
Among its 5 most recently registered devices, Von Zeppelin GmbH has devices listed in FDA 510(k) (5 devices).
What risk classes do Von Zeppelin GmbH's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Von Zeppelin GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Von Zeppelin GmbH in the registry?
The most recently registered devices listed for Von Zeppelin GmbH include PERNECZKY ANEURYSM CLIP, INSTRUMENTS FOR NEUROLOGICAL SURGERY, PERNECZKY CLIP APPLIER/REMOVER and ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM.