Medical Device Manufacturer · US , Murray , KY

Vivos Therapeutics, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022
2
Total
2
Cleared
0
Denied

Vivos Therapeutics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Murray, US.

Last cleared in 2023. Active since 2022. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Vivos Therapeutics, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Colette Cozean, PHD and Eyedeas Company.

FDA 510(k) Regulatory Record - Vivos Therapeutics, Inc.
2 devices
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