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Jeneric/Pentron, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
78
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K020499BOND-3 ADHESIVEApril 22, 2002
K013543BOND-1 C & BFebruary 22, 2002
K013542DENTIN CONDITIONING AND ADHESIVE SYSTEM (BOND-1)February 14, 2002
K012231AVANTE MICRO CRYSTAL SYSTEMAugust 23, 2001
K011748FIRST FILL R.C.S.August 3, 2001
K010957QUELL DESENSITIZERJune 25, 2001
K011331JP CAST 40June 22, 2001
K011330JP CAST 50June 22, 2001
K011362GOLD CORE 73 LSMay 29, 2001
K010044COSMICFebruary 9, 2001
K003683AVANTE CURELIGHTJanuary 11, 2001
K002854GOLD CORE POST SOLDERDecember 20, 2000
K002815GOLD CORE HF PRE SOLDERDecember 19, 2000
K003039GOLD CORE IIDecember 5, 2000
K003037JEWEL CAST IIIDecember 5, 2000
K003011SELF ETCH BONDING PRIMERNovember 28, 2000
K001623SCULPTURE FLOWJuly 11, 2000
K001218CORRECT PLUSJuly 5, 2000
K001051RX EVERESTApril 28, 2000
K994359BOND 1 C & BMarch 21, 2000