Medical Device Manufacturer · CH , Zurich

Sonova AG

2 submissions · 2 cleared · Since 2023
2
Total
2
Cleared
0
Denied

Sonova AG — FDA 510(k) Submissions

Sonova AG has submitted 2 FDA 510(k) premarket notifications since 2023, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Self-fitting Air-conduction Hearing Aid, Over The Counter, Hearing Aid, Air-conduction, Prescription . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Ear, Nose, Throat 2