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Gentex Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K080117PATIENT ISOLATION UNIT, MODEL G019-1000January 30, 2009
K800521THE LENS OR OMMI-GARDMarch 12, 1980
K772024RX LENS SERIESNovember 9, 1977