Lexington International, LLC - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Lexington International, LLC has 8 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 8 cleared submissions from 2007 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lexington International, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lexington International, LLC
8 devices
Cleared
Jun 20, 2018
HairMax Laser
General & Plastic Surgery
77d
Cleared
Dec 01, 2014
HairMax LaserComb, HairMax LaserComb
General & Plastic Surgery
80d
Cleared
Sep 26, 2011
HAIRMAX LASERCOMB
General & Plastic Surgery
26d
Cleared
Aug 16, 2011
HAIRMAX DUAL 12
General & Plastic Surgery
57d
Cleared
May 27, 2011
HAIRMAX LASERCOMB
General & Plastic Surgery
121d
Cleared
Apr 06, 2011
HAIRMAX LASERCOMB
General & Plastic Surgery
140d
Cleared
Nov 23, 2009
HAIRMAX LASERCOMB
General & Plastic Surgery
11d
Cleared
Jan 18, 2007
HAIRMAX LASERCOMB
General & Plastic Surgery
346d