W&H Dentalwerk Bürmoos GmbH
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2026-07-31
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253655 | Angled Screwdriver MED (M-SD090) | DZI | 2026-07-31 | View |
| 510(k) | K242179 | Synea Fusion Handpieces (Intensiv & Profin) | EFB | 2025-02-28 | View |
No matching devices.