Palomar Medical Technologies, Inc. is one of 5218 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Palomar Medical Technologies, Inc. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Palomar Medical Technologies, Inc. has 24 FDA 510(k) cleared general & plastic surgery devices. Based in Cary, US.
Historical record: 24 cleared submissions from 2000 to 2013.
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.
Palomar Medical Technologies, Inc. — FDA 510(k) Products and Clearance History
24 devices
Cleared
May 03, 2013
QYAG LASER SYSTEM
General & Plastic Surgery
91d
Cleared
May 23, 2012
PALOMAR VECTUS LASER
General & Plastic Surgery
83d
Cleared
Jun 22, 2011
PALOMAR ICON (TM) AESTHETIC SYSTEM
General & Plastic Surgery
83d
Cleared
Mar 17, 2011
PRIMUS AESTHETIC PLATFORM
General & Plastic Surgery
91d
Cleared
Sep 01, 2010
LUX1540, LUX1440 & LUX2940 LASER HANDPIECES
General & Plastic Surgery
92d
Cleared
Mar 29, 2010
ARTISAN AESTHETIC SYSTEM
General & Plastic Surgery
59d
Cleared
Nov 20, 2009
PALOMAR LUX1540 HANDPIECE
General & Plastic Surgery
297d
Cleared
Jul 03, 2007
MODIFICATION TO PALOMAR LUXIR HANDPIECE
General & Plastic Surgery
153d
Cleared
Feb 09, 2007
PALOMAR LUX2940 HANDPIECE
General & Plastic Surgery
72d
Cleared
Dec 07, 2006
ABC HAIR REMOVAL SYSTEM
General & Plastic Surgery
254d
Cleared
Dec 06, 2006
PALOMAR Q-YAG 5 ND:YAG LASER SYSTEM
General & Plastic Surgery
196d
Cleared
Mar 23, 2006
PALOMAR LUX1540 HANDPIECE
General & Plastic Surgery
45d