FDA applicant
Zimmer Dental, Inc.
FDA records 40 decisions for Zimmer Dental, Inc. (Carlsbad, CA) from 2005 to 2017: 40 510(k) clearances. Most are in product codes NHA (Abutment, Implant, Dental, Endosseous) and DZE (Implant, Endosseous, Root-Form). Its devices cite 75 predicates, 36 of them its own earlier devices. 30 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Zimmer Dental, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2017
2026 so far, outlined.
Recalls per year
1in 2018
Class I Class II/III not classified
Planning a device like Zimmer Dental, Inc.’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) ReportOther applicant names beginning “Zimmer”
FDA records each applicant name separately; these may or may not be the same firm.