Photo Medex, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Photo Medex, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Photo Medex, Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Carlsbad, US.
Historical record: 10 cleared submissions from 2001 to 2008.
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.
FDA 510(k) Regulatory Record - Photo Medex, Inc.
10 devices
Cleared
Oct 28, 2008
LASERPRO 810, 940 AND 980 DIODE LASER SYSTEMS
General & Plastic Surgery
41d
Cleared
Mar 05, 2008
XTRAC ULTRA 2, MODEL AL10000
General & Plastic Surgery
70d
Cleared
Aug 09, 2005
VTRAC EXCIMER LAMP SYSTEM
General & Plastic Surgery
69d
Cleared
Oct 14, 2004
XTRAC XL, MODEL AL8000
General & Plastic Surgery
87d
Cleared
May 05, 2004
LASERPRO DIODE LASER SYSTEMS, MODELS 810, 940 & 980
General & Plastic Surgery
89d
Cleared
Apr 02, 2004
LASERPRO CO2 CARBON DIOXIDE LASER SYSTEM
General & Plastic Surgery
60d
Cleared
Aug 01, 2003
XTRACXL PLUS EXCIMER LASER SYSTEM, MODEL AL7000
General & Plastic Surgery
86d
Cleared
May 16, 2002
XTRAC EXCIMER LASER SYSTEM, MODEL AL7000
General & Plastic Surgery
62d
Cleared
Aug 02, 2001
XTRAC EXCIMER LASER SYSTEM, MODEL AL 7000
General & Plastic Surgery
87d
Cleared
Mar 01, 2001
XTRAC EXCIMER LASER SYSTEM, MODEL AL7000
General & Plastic Surgery
90d