FDA applicant
Von Zeppelin GmbH
FDA records 5 decisions for Von Zeppelin GmbH (Pullach, DE) from 1990 to 2002: 5 510(k) clearances. Most are in product codes HAE (Rongeur, Manual) and HBB (Motor, Drill, Pneumatic). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Von Zeppelin GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Von Zeppelin GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Von Zeppelin GmbH’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report