# Gentex Corporation

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1977–2009): 3 510(k) clearances
- Product codes: HQG (2), LGM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K080117: Patient Isolation Unit, Model G019-1000 (Jan 30, 2009)
- K800521: The Lens or Ommi-Gard (Mar 12, 1980)
- K772024: RX Lens Series (Nov 9, 1977)

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