Medical Device Manufacturer · US , Carmel , IN

Omnia Spa

3 submissions · 3 cleared · Since 2011
3
Total
3
Cleared
0
Denied

Omnia Spa — FDA 510(k) Submissions

Omnia Spa has submitted 3 FDA 510(k) premarket notifications since 2011, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene, Gown, Surgical . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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All3 General & Plastic Surgery 2 General Hospital 1