510(k) K222836 · NHA Abutment, Implant, Dental, Endosseous
Straumann® Variobase® Abutments and Straumann® n!ce® Zirconia discs
| Applicant | Institut Straumann AG, Basel, CH |
| Decision | Substantially Equivalent, May 15, 2023 |
| Received | Sep 20, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222836
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 29, 2026 | Straumann USA LLC Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158.
Endosseous Dental Implant Abutments Open, Classified |
NHA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.