Lutronic Aesthetic
Country not established
- Devices
- 1
What Lutronic Aesthetic makes
Lutronic Aesthetic manufactures the MOSAIC 3D, a surgical laser system designed for precision tissue treatment in medical procedures.
The MOSAIC 3D 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
MOSAIC 3D (Surgical Laser) Ref K233550
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lutronic Aesthetic have in the registry?
The registry currently lists 1 device for Lutronic Aesthetic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lutronic Aesthetic's devices?
Among its 1 most recently registered device, Lutronic Aesthetic has devices listed in FDA 510(k) (1 device).
What risk classes do Lutronic Aesthetic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lutronic Aesthetic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lutronic Aesthetic in the registry?
The most recently registered devices listed for Lutronic Aesthetic include MOSAIC 3D (Surgical Laser).