Von Zeppelin GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Von Zeppelin GmbH - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Von Zeppelin GmbH has 5 FDA 510(k) cleared medical devices. Based in Pullach, DE.
Historical record: 5 cleared submissions from 1990 to 2002. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Von Zeppelin GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Von Zeppelin GmbH
5 devices
Cleared
Jan 25, 2002
ZMM 2000 ZEPPELIN MILLENNIUM MOTORDRILL SYSTEM
Neurology
130d
Cleared
Oct 08, 1996
PERNECZKY CLIP APPLIER/REMOVER
Neurology
364d
Cleared
Dec 11, 1990
INTERVERTEBRAL DISC RONGEUR
Neurology
146d
Cleared
Aug 17, 1990
PERNECZKY ANEURYSM CLIP
Neurology
150d
Cleared
Jul 23, 1990
INSTRUMENTS FOR NEUROLOGICAL SURGERY
Neurology
125d