Verilux
Country not established
- Devices
- 1
What Verilux makes
Verilux manufactures the CLEARWAVE Phototherapy System for Acne (Model CWST2), a device designed to treat acne vulgaris using controlled light therapy.
The CLEARWAVE Phototherapy System for Acne is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Verilux have in the registry?
The registry currently lists 1 device for Verilux. Devices recorded under merged duplicate company entries are counted once.
Which registries list Verilux's devices?
Among its 1 most recently registered device, Verilux has devices listed in FDA 510(k) (1 device).
What risk classes do Verilux's devices fall under?
Among its 1 most recently registered device, the classes recorded for Verilux's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Verilux in the registry?
The most recently registered devices listed for Verilux include CLEARWAVE PHOTOTHERAPY SYSTEM FOR ACNE, MODEL: CWST2.