Luxsano AB
Country not established
- Devices
- 1
What Luxsano AB makes
Luxsano AB manufactures the OMNILIGHT Fluorescent Pulsed Light System, a device designed for medical-grade photodynamic therapy and skin rejuvenation treatments using pulsed fluorescent light technology.
The OMNILIGHT Fluorescent Pulsed Light System is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Omnilight Fluorescent Pulsed Light System Ref K032191
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Luxsano AB have in the registry?
The registry currently lists 1 device for Luxsano AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luxsano AB's devices?
Among its 1 most recently registered device, Luxsano AB has devices listed in FDA 510(k) (1 device).
What risk classes do Luxsano AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Luxsano AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luxsano AB in the registry?
The most recently registered devices listed for Luxsano AB include OMNILIGHT FLUORESCENT PULSED LIGHT SYSTEM.