Vivos Therapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vivos Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: C.A.R.E. Appliance (DNA, mRNA, mmRNA), DNA Appliance
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