Medical Device Manufacturer · US , Wallingford , CT

Jeneric/Pentron, Inc. - FDA 510(k) Cleared Devices

78 submissions · 78 cleared · Since 1988

78

Total

78

Cleared

0

Denied

77 devices

76-77 of 77

Cleared Dec 07, 1988

FIBERLITE, FIBERLITE HS AND FIBERSEAL

Cleared Jun 17, 1988

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