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

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.

29 devices
1–12 of 29
XERF
K251327 · GEI Electrosurgical, Cutting & Coagulation & Accessories · General & Plastic Surgery
Aug 2025 103d
eCO2 3D
K244060 · ONG Powered Laser Surgical Instrument With Microbeamfractional Output · General & Plastic Surgery
Jul 2025 212d
CoreLevee
K213748 · NGX Stimulator, Muscle, Powered, For Muscle Conditioning · Physical Medicine
Oct 2022 318d
HOLLYWOOD SPECTRA Laser System
K213569 · GEX Powered Laser Surgical Instrument · General & Plastic Surgery
Feb 2022 87d
DermaV Laser System
K203788 · GEX Powered Laser Surgical Instrument · General & Plastic Surgery
Mar 2021 88d
CLARITY II Laser System
K183566 · GEX Powered Laser Surgical Instrument · General & Plastic Surgery
Jun 2019 175d
LUTRONIC GENIUS Radiofrequency System
K180945 · GEI Electrosurgical, Cutting & Coagulation & Accessories · General & Plastic Surgery
Dec 2018 243d
PICOPLUS Laser System
K173700 · GEX Powered Laser Surgical Instrument · General & Plastic Surgery
Jun 2018 197d
LASEMD Laser System
K171009 · GEX Powered Laser Surgical Instrument · General & Plastic Surgery
Jun 2017 80d
ACTION II Laser System
K163196 · GEX Powered Laser Surgical Instrument · General & Plastic Surgery
May 2017 190d
R:GEN Laser System
K153769 · HQF Laser, Ophthalmic · Ophthalmic
Oct 2016 280d
ADVANTAGE
K141555 · GEX Powered Laser Surgical Instrument · General & Plastic Surgery
Nov 2014 147d
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