Dermawave, LLC
Country not established
- Devices
- 1
What Dermawave, LLC makes
Dermawave, LLC manufactures the DERMAWAVE 5000 COMBI MAX SYSTEM, a fractional radiofrequency device designed for skin remodeling and tissue tightening procedures.
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Dermawave 5000 Combi Max System Ref K040121
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermawave, LLC have in the registry?
The registry currently lists 1 device for Dermawave, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermawave, LLC's devices?
Among its 1 most recently registered device, Dermawave, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Dermawave, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dermawave, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermawave, LLC in the registry?
The most recently registered devices listed for Dermawave, LLC include DERMAWAVE 5000 COMBI MAX SYSTEM.