Medical Device Manufacturer · US , North Reading , MA

Lutronic Corporation - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 2007

Recent clearances: XERF, eCO2 3D, CoreLevee

29

Total

29

Cleared

0

Denied

FDA 510(k) Regulatory Record - Lutronic Corporation Ophthalmic ✕

1 devices

1-1 of 1

Cleared Oct 05, 2016

R:GEN Laser System

Ophthalmic · 280d