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Pentron Clinical Technologies

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K091512BUILD-IT LIGHT CUREOctober 30, 2009
K081887LUTE-IT II VENEER CEMENT, MODEL NO6August 29, 2008
K072830RM BOND, MODEL J032December 4, 2007
K072480GENERATION 8 SE ADHESIVENovember 21, 2007
K072545ARTISTE SE FLOWABLE COMPOSITE, MODEL N280October 26, 2007
K071500NANO-BOND II ADHESIVE SYSTEMAugust 10, 2007
K060889SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SEOctober 27, 2006
K060698CEMENT-IT ALL PURPOSE, MODEL N97May 10, 2006
K052106SIMILE FLOWOctober 31, 2005
K052349AVANTE LED CURING UNIT, MODEL N44October 21, 2005
K023818FIBERFILL AGPApril 3, 2003
K023819FIBERFILL SGPMarch 26, 2003
K022150TRIONOMERAugust 21, 2002