Lutronic Vision, Inc.
Country not established
- Devices
- 1
What Lutronic Vision, Inc. makes
Lutronic Vision, Inc. manufactures the R:GEN, a device designed for radiofrequency-based skin treatments, including skin tightening and collagen stimulation.
The company’s portfolio is regulated under FDA Class II devices, with the R:GEN authorised via a 510(k) clearance. The manufacturer is based in the United States.
Catalogue
R:gen Ref K220974
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lutronic Vision, Inc. have in the registry?
The registry currently lists 1 device for Lutronic Vision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lutronic Vision, Inc.'s devices?
Among its 1 most recently registered device, Lutronic Vision, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lutronic Vision, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lutronic Vision, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lutronic Vision, Inc. in the registry?
The most recently registered devices listed for Lutronic Vision, Inc. include R:GEN.