FDA applicant
Cendres & Metaux SA
FDA records 8 decisions for Cendres & Metaux SA (Biel/Bienne, CH) from 2010 to 2020: 8 510(k) clearances. Most are in product codes NHA (Abutment, Implant, Dental, Endosseous) and EIH (Powder, Porcelain). Its devices cite 21 predicates, 8 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Cendres+Metaux SA”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Cendres & Metaux SA’s devices, and how often a recall has named them.
FDA decisions per year
1in 2020
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2010.
Planning a device like Cendres & Metaux SA’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