Pentron Clinical Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pentron Clinical Technologies - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Pentron Clinical Technologies has 13 FDA 510(k) cleared dental devices. Based in Wallingford, US.
Historical record: 13 cleared submissions from 2002 to 2009.
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 - Pentron Clinical Technologies
13 devices
Cleared
Oct 30, 2009
BUILD-IT LIGHT CURE
Dental
162d
Cleared
Aug 29, 2008
LUTE-IT II VENEER CEMENT, MODEL NO6
Dental
58d
Cleared
Dec 04, 2007
RM BOND, MODEL J032
Dental
62d
Cleared
Nov 21, 2007
GENERATION 8 SE ADHESIVE
Dental
78d
Cleared
Oct 26, 2007
ARTISTE SE FLOWABLE COMPOSITE, MODEL N280
Dental
46d
Cleared
Aug 10, 2007
NANO-BOND II ADHESIVE SYSTEM
Dental
71d
Cleared
Oct 27, 2006
SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE
Dental
210d
Cleared
May 10, 2006
CEMENT-IT ALL PURPOSE, MODEL N97
Dental
55d
Cleared
Oct 31, 2005
SIMILE FLOW
Dental
89d
Cleared
Oct 21, 2005
AVANTE LED CURING UNIT, MODEL N44
Dental
53d
Cleared
Apr 03, 2003
FIBERFILL AGP
Dental
139d
Cleared
Mar 26, 2003
FIBERFILL SGP
Dental
131d