Gentex Corporation

3 FDA 510(k) medical device clearances.

Top product codes for Gentex Corporation

HQG — Ophthalmic 2 devices
LGM — General Hospital 1 device

Recent clearances by Gentex Corporation

K080117 — PATIENT ISOLATION UNIT, MODEL G019-1000 LGM · 2009-01-30
K800521 — THE LENS OR OMMI-GARD HQG · 1980-03-12
K772024 — RX LENS SERIES HQG · 1977-11-09

Data sourced from openFDA. This site is unofficial and independent of the FDA.