Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I)
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- Devices
- 1
What Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I) makes
Vivos Therapeutics, Inc. manufactures an mRNA-based appliance designed for therapeutic delivery, targeting localized treatment applications.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The manufacturer is based in the United States.
Catalogue
mmRNA appliance Ref K210203
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I) have in the registry?
The registry currently lists 1 device for Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I). Devices recorded under merged duplicate company entries are counted once.
Which registries list Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I)'s devices?
Among its 1 most recently registered device, Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I) has devices listed in FDA 510(k) (1 device).
What risk classes do Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I) in the registry?
The most recently registered devices listed for Vivos Therapeutics, Inc. (Formerly Vivos Biotechnologies, I) include mmRNA appliance.