K253655
- 510(k) number
- K253655
- Device name
- Angled Screwdriver MED (M-SD090)
- Applicant
- W&H Dentalwerk Bürmoos GmbH AT
- Product code
- DZI — Drill, Bone, Powered
- Decision date
- 2026-07-31
- Date received
- 2025-11-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K253655.pdf
Official FDA record: K253655
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.