Medical Device Manufacturer · US , Wallingford , CT

Pentron Clinical Technologies - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2002

Recent clearances: BUILD-IT LIGHT CURE, LUTE-IT II VENEER CEMENT, MODEL NO6, RM BOND, MODEL J032

View 13 510(k) Devices ↓

13

Total

13

Cleared

0

Denied

FDA 510(k) Regulatory Record - Pentron Clinical Technologies Dental ✕

13 devices

1-12 of 13

Cleared Oct 30, 2009

BUILD-IT LIGHT CURE

Cleared Aug 29, 2008

LUTE-IT II VENEER CEMENT, MODEL NO6

Cleared Dec 04, 2007

RM BOND, MODEL J032

Cleared Nov 21, 2007

GENERATION 8 SE ADHESIVE

Cleared Oct 26, 2007

ARTISTE SE FLOWABLE COMPOSITE, MODEL N280

Cleared Aug 10, 2007

NANO-BOND II ADHESIVE SYSTEM

Cleared Oct 27, 2006

SE EPIPHANY ROOT CANAL SEALANT, MODEL N59SE

Cleared May 10, 2006

CEMENT-IT ALL PURPOSE, MODEL N97

Cleared Oct 31, 2005

Cleared Oct 21, 2005

AVANTE LED CURING UNIT, MODEL N44

Cleared Apr 03, 2003

Cleared Mar 26, 2003