Lutronic Corporation - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Lutronic Corporation has 29 FDA 510(k) cleared general & plastic surgery devices. Based in North Reading, US.
Latest FDA clearance: Aug 2025. Active since 2007.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Lutronic Corporation
29 devices
Cleared
Aug 11, 2025
XERF
General & Plastic Surgery
103d
Cleared
Jul 31, 2025
eCO2 3D
General & Plastic Surgery
212d
Cleared
Oct 14, 2022
CoreLevee
Physical Medicine
318d
Cleared
Feb 04, 2022
HOLLYWOOD SPECTRA Laser System
General & Plastic Surgery
87d
Cleared
Mar 26, 2021
DermaV Laser System
General & Plastic Surgery
88d
Cleared
Jun 14, 2019
CLARITY II Laser System
General & Plastic Surgery
175d
Cleared
Dec 10, 2018
LUTRONIC GENIUS Radiofrequency System
General & Plastic Surgery
243d
Cleared
Jun 19, 2018
PICOPLUS Laser System
General & Plastic Surgery
197d
Cleared
Jun 23, 2017
LASEMD Laser System
General & Plastic Surgery
80d
Cleared
May 24, 2017
ACTION II Laser System
General & Plastic Surgery
190d
Cleared
Oct 05, 2016
R:GEN Laser System
Ophthalmic
280d
Cleared
Nov 06, 2014
ADVANTAGE
General & Plastic Surgery
147d