Erchonia Corporation was the first company to obtain FDA Market clearance for a low –level laser. The clearance, received on January 17, 2002, was the culmination of 2 years of efforts and two IRB approved studies. Needless to say, we blazed the trail for low level laser and established a standing prescient for ourselves, that being – all Erchonia Corporation indications for use, would be verifiable through clinical research.

At present we have the following 510(K) market clearances:

TUCO Erchonia PL3000 -Neck and Shoulder Pain

Erchonia EML Laser  - Laser Assisted Liposuction

Erchonia EVRL Laser - Acne

Erchonia EML Laser - Breast Augmentation

Zerona Laser - Non Invasive Body Contouring