Cabochon Aesthetics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Cabochon Aesthetics, Inc. makes
Cabochon Aesthetics, Inc. manufactures the Cabochon System, a medical device designed for aesthetic procedures.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Cabochon System Ref DEN110004
Regimes: De Novo Registry: De NovoCabochon System Ref K134010
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cabochon Aesthetics, Inc. have in the registry?
The registry currently lists 2 devices for Cabochon Aesthetics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cabochon Aesthetics, Inc.'s devices?
Among its 2 most recently registered devices, Cabochon Aesthetics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cabochon Aesthetics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cabochon Aesthetics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cabochon Aesthetics, Inc. in the registry?
The most recently registered devices listed for Cabochon Aesthetics, Inc. include CABOCHON SYSTEM.