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.

Hgm, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

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

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