Hgm Medical Laser Systems, Inc. is one of 15143 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hgm Medical Laser Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODEL PC ARGON ION LASER, LITESPOT(TM) LASER INDIRECT OPHTHALMOSCOPE, COMPAC A, ELITE A, ELITE A PLUS, SURGICA A
18
Total
18
Cleared
0
Denied
Hgm Medical Laser Systems, Inc. has 18 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 18 cleared submissions from 1988 to 1992. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hgm Medical Laser Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Boston Scientific as regulatory consultant.
FDA 510(k) Regulatory Record - Hgm Medical Laser Systems, Inc.
18 devices
Cleared
Oct 06, 1992
MODEL PC ARGON ION LASER
General & Plastic Surgery
202d
Cleared
Jan 06, 1992
LITESPOT(TM) LASER INDIRECT OPHTHALMOSCOPE
Ophthalmic
90d
Cleared
Oct 17, 1991
COMPAC A, ELITE A, ELITE A PLUS, SURGICA A
General & Plastic Surgery
69d
Cleared
Sep 13, 1991
AIR ARGON ION LASERS VARIOUS MODELS
General & Plastic Surgery
88d
Cleared
Aug 09, 1991
HGM COMBINATION ND:YAG & SOLID STATE GREEN
General & Plastic Surgery
198d
Cleared
Jul 17, 1991
MODELS 5,8,20,20S ARGON ION LASERS
General & Plastic Surgery
44d
Cleared
Jun 24, 1991
HGM ARGON ION & SOLID LIGHT LASER FOR DENTISTRY
General & Plastic Surgery
131d
Cleared
Jun 11, 1991
PHOTCOAGULATOR KR-568 LASER SPECTRUM ELITE K1
Gastroenterology & Urology
90d
Cleared
May 31, 1991
SURGICA(TM) H
General & Plastic Surgery
88d
Cleared
Apr 25, 1991
COMPAC(TM) DIODE LASERS
Ophthalmic
191d
Cleared
Feb 19, 1991
ENDOCOAGULATOR KRS568(TM) LASER
General & Plastic Surgery
126d
Cleared
Dec 19, 1990
SERIES 1990 ARGON SURGICAL LASERS, E1,E6,E14&E20A
General & Plastic Surgery
89d