K253776
- 510(k) number
- K253776
- Device name
- Implantmed Plus II & Piezomed Plus II Module
- Applicant
- W&H Dentalwerk Buermoos GmbH AT
- Product code
- DZI — Drill, Bone, Powered
- Decision date
- 2026-06-18
- Date received
- 2025-11-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K253776.pdf
Official FDA record: K253776
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.