510(k) K253776 ยท DZI Drill, Bone, Powered
Implantmed Plus II & Piezomed Plus II Module
| Applicant | W&H Dentalwerk Buermoos GmbH, Buermoos, AT |
| Decision | Substantially Equivalent, Jun 18, 2026 |
| Received | Nov 26, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253776
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.