510(k) Report

FDA applicant

Bonyf AG

Silver Creek, NY1 decision2006–20060 recalls

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, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

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.

FIG. 1 — Bonyf AG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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