Synea Fusion Handpieces (Intensiv & Profin)
Feb 2025
218d
W&H Dentalwerk B?rmoos GmbH
1
Total
1
Cleared
0
Denied
W&H Dentalwerk B?rmoos GmbH — FDA 510(k) Submissions
W&H Dentalwerk B?rmoos GmbH has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Handpiece, Air-powered, Dental . Use the specialty filter in the sidebar to narrow results.
1 devices