510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931072Substantially Equivalent

Hgm Illuminating/aspirating Endoocular Probe

Hgm, Inc., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931072 is the FDA 510(k) clearance record for HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE, a class II device, cleared for Hgm, Inc. on under FDA product code HJM (Transilluminator, Ac-Powered). FDA records list 21 510(k) clearances for Hgm, Inc., from to . As of , FDA records show no recalls naming K931072.

Clearance record

Decision date
Received
(618 days to decision)
Product code
HJM Transilluminator, Ac-Powered
Regulation
21 CFR 886.1945
Device class
Class II
Review panel
Ophthalmic
Applicant
Hgm, Inc. 3959 W. 1820 S., Salt Lake City UT
510(k) summary
Statement
Third party review
No

Clearances, product code HJM

Trailing 12 months

FDA records hold no clearances under product code HJM in the trailing twelve months.

FDA records show no clearances under product code HJM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HJM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260