Medical Device Manufacturer · US , North Reading , MA

Lutronic Corporation - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 2007
29
Total
29
Cleared
0
Denied

FDA 510(k) cleared devices by Lutronic Corporation General & Plastic Surgery ✕

26 devices
1-12 of 26
Cleared Aug 11, 2025
XERF
K251327 · GEI
General & Plastic Surgery · 103d
Cleared Jul 31, 2025
eCO2 3D
K244060 · ONG
General & Plastic Surgery · 212d
Cleared Feb 04, 2022
HOLLYWOOD SPECTRA Laser System
K213569 · GEX
General & Plastic Surgery · 87d
Cleared Mar 26, 2021
DermaV Laser System
K203788 · GEX
General & Plastic Surgery · 88d
Cleared Jun 14, 2019
CLARITY II Laser System
K183566 · GEX
General & Plastic Surgery · 175d
Cleared Dec 10, 2018
LUTRONIC GENIUS Radiofrequency System
K180945 · GEI
General & Plastic Surgery · 243d
Cleared Jun 19, 2018
PICOPLUS Laser System
K173700 · GEX
General & Plastic Surgery · 197d
Cleared Jun 23, 2017
LASEMD Laser System
K171009 · GEX
General & Plastic Surgery · 80d
Cleared May 24, 2017
ACTION II Laser System
K163196 · GEX
General & Plastic Surgery · 190d
Cleared Nov 06, 2014
ADVANTAGE
K141555 · GEX
General & Plastic Surgery · 147d
Cleared Nov 22, 2013
CLARITY LPC LASER SYSTEM
K130199 · GEX
General & Plastic Surgery · 298d
Cleared Jun 25, 2013
INFINI RADIOFREQUENCY SYSTEM
K121481 · GEI
General & Plastic Surgery · 403d
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