1980’s - The HairMax® LaserComb was designed and developed in Australia. The founding director of Lexington International, LLC, Henry Pearl was a pioneer in the use of laser technology at a leading skin and hair care clinic and research center in Sydney, Australia. 2000 - The company was established in the U.S.A. to develop and market this revolutionary device. 2002 - Lexington International introduced the HairMax LaserComb. Key Clinical Study The results of the key clinical study performed with the HairMax LaserComb which led to this FDA Clearance to market was published in the May 2009 Issue of Clinical Drug Investigation. For detailed results of this study, Please Click Here

FDA Submission & Clearance

January 2006 - 510K filing for the HairMax submitted to FDA.
January 2007 - Marketing clearance granted by the FDA .
For FDA Submission & Clearance Details, Please Click Here


Official Indication

“To promote hair growth in males with androgenetic alopecia who have Norwood Hamilton Classifications of IIa to V and Fitzpatrick Skin Types I to IV”


Strict Quality Standards

The HairMax LaserComb is assembled in the USA under strict quality control standards and complies with all applicable laser safety standards.


The HairMax LaserComb is the only medical hair growth device on the market with FDA marketing clearance for the treatment of certain classes of Androgenetic Alopecia in males.