Solx, Inc.
Country not established
- Devices
- 1
What Solx, Inc. makes
Solx, Inc. manufactures the SOLX 790 Titanium Sapphire Laser, a medical laser device designed for dermatological and cosmetic procedures, including hair removal and skin resurfacing.
The SOLX 790 Titanium Sapphire Laser is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Solx 790 Titanium Sapphire Laser Ref K081774
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Solx, Inc. have in the registry?
The registry currently lists 1 device for Solx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Solx, Inc.'s devices?
Among its 1 most recently registered device, Solx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Solx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Solx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Solx, Inc. in the registry?
The most recently registered devices listed for Solx, Inc. include SOLX 790 TITANIUM SAPPHIRE LASER.