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Vivos Therapeutics INC.

Also registered as Vivos Therapeutics

Country not established FDA establishment FEI 3022315836

Devices
3
Registrations
FDA
FDA recalls
0

Catalogue3

Newest first, rows 1-3 of 3

  • DNA Appliance Ref K234089

    Class II
    Active 510(k) 510(k) II
  • DNA Appliance Ref K222872

    Class II
    Active 510(k) 510(k) II
  • C.A.R.E. Appliance (DNA, mRNA, mmRNA) Ref K230947

    Class II
    Active 510(k) 510(k) II

Company details

FDA FEI number
3022315836
Address
300 S 5th Street, Murray, KY, 42071

Frequently asked questions

How many devices does Vivos Therapeutics INC. have in the registry?

The registry currently lists 3 devices for Vivos Therapeutics INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vivos Therapeutics INC.'s devices?

Among its 3 most recently registered devices, Vivos Therapeutics INC. has devices listed in FDA 510(k) (3 devices).

What risk classes do Vivos Therapeutics INC.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Vivos Therapeutics INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Vivos Therapeutics INC. in the registry?

The most recently registered devices listed for Vivos Therapeutics INC. include DNA Appliance and C.A.R.E. Appliance (DNA, mRNA, mmRNA).

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.