Jeneric/Pentron, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jeneric/Pentron, Inc. - FDA 510(k) Cleared Devices
78
Total
78
Cleared
0
Denied
Jeneric/Pentron, Inc. has 78 FDA 510(k) cleared dental devices. Based in Wallingford, US.
Historical record: 78 cleared submissions from 1988 to 2002.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jeneric/Pentron, Inc.
78 devices
Cleared
Apr 22, 2002
BOND-3 ADHESIVE
Dental
67d
Cleared
Feb 22, 2002
BOND-1 C & B
Dental
128d
Cleared
Feb 14, 2002
DENTIN CONDITIONING AND ADHESIVE SYSTEM (BOND-1)
Dental
120d
Cleared
Aug 23, 2001
AVANTE MICRO CRYSTAL SYSTEM
Dental
38d
Cleared
Aug 03, 2001
FIRST FILL R.C.S.
Dental
58d
Cleared
Jun 25, 2001
QUELL DESENSITIZER
Dental
87d
Cleared
Jun 22, 2001
JP CAST 50
Dental
51d
Cleared
Jun 22, 2001
JP CAST 40
Dental
51d
Cleared
May 29, 2001
GOLD CORE 73 LS
Dental
26d
Cleared
Feb 09, 2001
COSMIC
Dental
35d
Cleared
Jan 11, 2001
AVANTE CURELIGHT
Dental
43d
Cleared
Dec 20, 2000
GOLD CORE POST SOLDER
Dental
100d
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