Lutronic Global
Country not established
- Devices
- 1
What Lutronic Global makes
Lutronic Global manufactures the LaseMD LEO Laser System, a device designed for non-ablative skin resurfacing and hair removal using fractional laser technology.
The LaseMD LEO Laser 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
LaseMD LEO Laser System Ref K192331
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lutronic Global have in the registry?
The registry currently lists 1 device for Lutronic Global. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lutronic Global's devices?
Among its 1 most recently registered device, Lutronic Global has devices listed in FDA 510(k) (1 device).
What risk classes do Lutronic Global's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lutronic Global's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lutronic Global in the registry?
The most recently registered devices listed for Lutronic Global include LaseMD LEO Laser System.