Medical Device Manufacturer · US , Salt Lake City , UT

Hgm, Inc. - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 1983

23

Total

23

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hgm, Inc. General & Plastic Surgery ✕

7 devices

1-7 of 7

Cleared Aug 11, 1995

General & Plastic Surgery · 211d

Cleared Sep 23, 1993

HGM SCANMAN PLUS

General & Plastic Surgery · 77d

Cleared Aug 19, 1993

Q-11 OPHTHALMIC LASER

General & Plastic Surgery · 147d

Cleared Jun 22, 1993

E-25 KRYPTON ION LASER (SURGICA K5)

General & Plastic Surgery · 140d

Cleared May 03, 1988

MODEL PC ARGON LASER

General & Plastic Surgery · 61d

Cleared Oct 13, 1987

ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASER

General & Plastic Surgery · 27d

Cleared Jul 23, 1985

HGM ENDOCOAGULATOR MODEL 8

General & Plastic Surgery · 92d