Medical Device Manufacturer · US , Salt Lake City , UT

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

23 submissions · 23 cleared · Since 1983

Total

Cleared

Denied

Hgm, Inc. has 23 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.

Historical record: 23 cleared submissions from 1983 to 1995.

Browse the FDA 510(k) cleared devices submitted by Hgm, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Hgm, Inc.

23 devices

1-12 of 23

Cleared Aug 11, 1995

SMART PLUG

K950120 · GEX

General & Plastic Surgery · 211d

Cleared Nov 10, 1994

HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE

K931072 · HJM

Ophthalmic · 618d

Cleared Mar 01, 1994

HGM ILLUMINATING IMAGING ENDOCULAR PROBE

General & Plastic Surgery · 77d

Cleared Aug 19, 1993

Q-11 OPHTHALMIC LASER

K931499 · GEX

General & Plastic Surgery · 147d

Cleared Aug 17, 1993

HGM ASPIRATING ENDOOCULAR(TM) PROBE

K925663 · HQF

Ophthalmic · 280d

Cleared Jun 22, 1993

E-25 KRYPTON ION LASER (SURGICA K5)

K930543 · GEX

General & Plastic Surgery · 140d

Cleared May 03, 1988

MODEL PC ARGON LASER

K880908 · GEX

General & Plastic Surgery · 61d

Cleared Oct 13, 1987

ENDOCOAGULATOR MODELS 8 AND 20 ARGON LASER

K873773 · GEX

General & Plastic Surgery · 27d

Cleared Aug 25, 1987

ENDOCOAGULATOR(TM) MODEL 20 ARGON LASER FOR UROLO.

K872630 · LNK

Gastroenterology & Urology · 50d

Cleared Jul 10, 1987

ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER

K870773 · LLF

Neurology · 134d

Cleared Jul 08, 1987

ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER

K871424 · LMS

Ear, Nose, Throat · 90d

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

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