Medical Device Manufacturer · US , Carmel , IN

Omnia Spa - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2011

Total

Cleared

Denied

Omnia Spa has 3 FDA 510(k) cleared medical devices. Based in Carmel, US.

Historical record: 3 cleared submissions from 2011 to 2018. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Omnia Spa Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Omnia Spa

3 devices

1-3 of 3