FDA 510(k) Applications Submitted by PENTRON CLINICAL TECHNOLOGIES

FDA 510(k) Number	Submission Date	Device Name	Applicant
K022150	07/02/2002	TRIONOMER	PENTRON CLINICAL TECHNOLOGIES
K023818	11/15/2002	FIBERFILL AGP	PENTRON CLINICAL TECHNOLOGIES
K023819	11/15/2002	FIBERFILL SGP	PENTRON CLINICAL TECHNOLOGIES
K071500	05/31/2007	NANO-BOND II ADHESIVE SYSTEM	PENTRON CLINICAL TECHNOLOGIES
K072480	09/04/2007	GENERATION 8 SE ADHESIVE	PENTRON CLINICAL TECHNOLOGIES
K060698	03/16/2006	CEMENT-IT ALL PURPOSE, MODEL N97	PENTRON CLINICAL TECHNOLOGIES
K060889	03/31/2006	SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE	PENTRON CLINICAL TECHNOLOGIES
K081887	07/02/2008	LUTE-IT II VENEER CEMENT, MODEL NO6	PENTRON CLINICAL TECHNOLOGIES
K052106	08/03/2005	SIMILE FLOW	PENTRON CLINICAL TECHNOLOGIES
K052349	08/29/2005	AVANTE LED CURING UNIT, MODEL N44	PENTRON CLINICAL TECHNOLOGIES
K072545	09/10/2007	ARTISTE SE FLOWABLE COMPOSITE, MODEL N280	PENTRON CLINICAL TECHNOLOGIES
K072830	10/03/2007	RM BOND, MODEL J032	PENTRON CLINICAL TECHNOLOGIES
K091512	05/21/2009	BUILD-IT LIGHT CURE	PENTRON CLINICAL TECHNOLOGIES