# Hgm, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 23 (1983–1995): 23 510(k) clearances
- Product codes: GEX (6), HQF (6), LNK (2), LMS (1), LLF (1), HHR (1), HJM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Lumenis, Inc.: 4 (https://510kreport.com/company/lumenis)
- Iridex Corp: 2 (https://510kreport.com/company/iridex)
- Accutech Medical Technologies, Inc.: 1 (https://510kreport.com/company/accutech-medical-technologies)
- Nidek, Inc.: 1 (https://510kreport.com/company/nidek)
- Innovatech Surgical, Inc.: 1 (https://510kreport.com/company/innovatech-surgical)
- Peregrine Surgical, Ltd.: 1 (https://510kreport.com/company/peregrine-surgical)
- Sterilmed, Inc.: 1 (https://510kreport.com/company/sterilmed)

## Its most-cited devices
- K931784: HGM Illuminating Imaging Endocular Probe (1994), cited by 4
- K931072: HGM Illuminating/Aspirating Endoocular Probe (1994), cited by 2
- K840590: Fleischman-Swartz Endo-Ocular Probe (1984), cited by 2
- K925663: HGM Aspirating Endoocular (TM) Probe (1993), cited by 1
- K930543: E-25 Krypton Ion Laser (Surgica K5) (1993), cited by 1
- K860358: Fleischman-Swartz Endo-Ocular Probe (Sterile) (1986), cited by 1

## Recent decisions
- K950120: Smart Plug (Aug 11, 1995)
- K931072: HGM Illuminating/Aspirating Endoocular Probe (Nov 10, 1994)
- K931784: HGM Illuminating Imaging Endocular Probe (Mar 1, 1994)
- K933333: HGM Scanman Plus (Sep 23, 1993)
- K931499: Q-11 Ophthalmic Laser (Aug 19, 1993)
- K925663: HGM Aspirating Endoocular (TM) Probe (Aug 17, 1993)
- K930543: E-25 Krypton Ion Laser (Surgica K5) (Jun 22, 1993)
- K880908: Model PC Argon Laser (May 3, 1988)

Source page: https://510kreport.com/company/hgm