Rejuveness Pharamceuticals, Inc.
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- Devices
- 1
What Rejuveness Pharamceuticals, Inc. makes
Rejuveness Pharmaceuticals, Inc. manufactures the REJUVENESS device, a Class I medical product designed for cosmetic or skin rejuvenation procedures.
The REJUVENESS device is regulated under the FDA’s 510(k) pathway as a Class I product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Rejuveness Ref K974380
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rejuveness Pharamceuticals, Inc. have in the registry?
The registry currently lists 1 device for Rejuveness Pharamceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rejuveness Pharamceuticals, Inc.'s devices?
Among its 1 most recently registered device, Rejuveness Pharamceuticals, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Rejuveness Pharamceuticals, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rejuveness Pharamceuticals, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rejuveness Pharamceuticals, Inc. in the registry?
The most recently registered devices listed for Rejuveness Pharamceuticals, Inc. include REJUVENESS.