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FDA 510(k) Applications Submitted by Kerr Corporation
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191548
06/12/2019
Nexus Universal Self-Cure
Kerr Corporation
K060472
02/23/2006
PREMISE FLOWABLE
KERR CORPORATION
K071251
05/04/2007
DEMI
KERR CORPORATION
K071429
05/23/2007
TI2200 TRANSILLUMINATION CABLE
KERR CORPORATION
K062519
08/28/2006
NEXUS 3
KERR CORPORATION
K073209
11/14/2007
MAXCEM 2
KERR CORPORATION
K123595
11/21/2012
NEXUS RMGI
KERR CORPORATION
K221255
05/02/2022
SimpliShade Bulk Fill, SimpliShade Bulk Fill Flow
Kerr Corporation
K162948
10/21/2016
Styptin, Hemogin-L, Hemodettes, and GingiGEL Aluminum Chloride Impregnated Retraction Cord/Materials
KERR CORPORATION
K160441
02/17/2016
Identic and KromaFaze Alginate Dental Impression Materials
KERR CORPORATION
K162164
08/03/2016
GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord
KERR CORPORATION
K182162
08/10/2018
OptiBond eXTRa Universal
Kerr Corporation
K162257
08/11/2016
P1145 Dental Restorative
Kerr Corporation
K162436
08/31/2016
EndoVac Pure
Kerr Corporation
K162536
09/12/2016
GingiKnit+, GingiBraid+, GingiBraid+ Shortcut, and UniBraid+ impregnated Aluminum Potassium Sulfate Retraction Cord
KERR CORPORATION
K163064
11/02/2016
Demi Ultra
KERR CORPORATION
K222830
09/19/2022
Rainbow 360
Kerr Corporation
K100083
01/12/2010
ESTHETICA
KERR CORPORATION
K110092
01/12/2011
TAKE 1 ADVANCED RIGID TRAY
KERR CORPORATION
K100347
02/12/2010
OPTIBOND SE
KERR CORPORATION
K110747
03/17/2011
TEMPFLEX
KERR CORPORATION
K091023
04/10/2009
METAMORPHOSIS
KERR CORPORATION
K101423
05/20/2010
OPTIBOND XTR
KERR CORPORATION
K101756
06/23/2010
TSC
KERR CORPORATION
K092176
07/21/2009
TAKE 1 ADVANCED RIGID TRAY
KERR CORPORATION
K102133
07/29/2010
GIRAFFE2
KERR CORPORATION
K102621
09/13/2010
SOLSTICE
KERR CORPORATION
K093484
11/09/2009
PREMISE FLOWABLE MODIFIED
KERR CORPORATION
K123468
11/09/2012
DEMI ULTRA
KERR CORPORATION
K103351
11/16/2010
DMC COMPOSITE 2
KERR CORPORATION
K102163
08/02/2010
REALSEAL XT SEALER
KERR CORPORATION
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