PRENUVO Inc.
Also registered as Prenuvo
United Statesfrom the FDA registration address FDA establishment FEI 3017297314
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Prenuvo Body Composition Ref K242825
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3017297314
- Address
- 2727 El Camino Real, Redwood City, CA, 94061
Frequently asked questions
How many devices does PRENUVO Inc. have in the registry?
The registry currently lists 1 device for PRENUVO Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list PRENUVO Inc.'s devices?
Among its 1 most recently registered device, PRENUVO Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do PRENUVO Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for PRENUVO Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PRENUVO Inc. in the registry?
The most recently registered devices listed for PRENUVO Inc. include Prenuvo Body Composition.