FDA applicant
Bonyf AG
FDA records 1 decision for Bonyf AG (Silver Creek, NY) in 2006: 1 510(k) clearance. All are in product code EFT (Cleanser, Denture, Over The Counter). 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 Bonyf AG’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Bonyf AG since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Bonyf AG’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