Kaylight Corporation
Country not established
- Devices
- 1
What Kaylight Corporation makes
Kaylight Corporation manufactures the Kenkowave Infrared Pain Treatment System, a device designed for non-invasive pain management using infrared technology.
The Kenkowave Infrared Pain Treatment System is classified as a Class II medical device in the US and is authorised via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Kenkowave Infrared Pain Treatment System Ref K033555
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kaylight Corporation have in the registry?
The registry currently lists 1 device for Kaylight Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kaylight Corporation's devices?
Among its 1 most recently registered device, Kaylight Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Kaylight Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kaylight Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kaylight Corporation in the registry?
The most recently registered devices listed for Kaylight Corporation include KENKOWAVE INFRARED PAIN TREATMENT SYSTEM.