MOSAIC 3D (Surgical Laser)
Jan 2024
60d
Lutronic Aesthetic
1
Total
1
Cleared
0
Denied
Lutronic Aesthetic — FDA 510(k) Submissions
Lutronic Aesthetic has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Powered Laser Surgical Instrument With Microbeamfractional Output . Use the specialty filter in the sidebar to narrow results.
1 devices