FDA applicant

Hgm, Inc.

Salt Lake City, UT23 decisions1983–19950 recalls

FDA records 23 decisions for Hgm, Inc. (Salt Lake City, UT) from 1983 to 1995: 23 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and HQF (Laser, Ophthalmic). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Hgm, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hgm, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hgm, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Hgm, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?