Vitage Led, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Vitage Led, Ltd. makes
Vitage Led, Ltd. manufactures the LightFusion LED System, a medical device designed for photodynamic and photothermal therapies, utilizing LED technology to deliver targeted light treatments for dermatological and aesthetic applications.
The LightFusion LED System 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
Lightfusion Led System Ref K162556
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vitage Led, Ltd. have in the registry?
The registry currently lists 1 device for Vitage Led, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitage Led, Ltd.'s devices?
Among its 1 most recently registered device, Vitage Led, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Vitage Led, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vitage Led, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitage Led, Ltd. in the registry?
The most recently registered devices listed for Vitage Led, Ltd. include LIGHTFUSION LED SYSTEM.