ClearanceBrief
Company ยท DE

Kaltenbach & Voigt GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2019. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EFAHandpiece, Belt And/Or Gear Driven, Dental3
EBWController, Foot, Handpiece And Cord2
EFBHandpiece, Air-Powered, Dental2
EIAUnit, Operative Dental2
NTKLight Transmission Caries Detector2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 23, 2019K182712DEXIS CariVu 3-in-1 by KaVo
Kaltenbach & Voigt GmbH, DE
NTK
Apr 10, 2019K181110PROPHYflex 4
Kaltenbach & Voigt GmbH, DE
EFB
Mar 17, 2017K163239SMARTmatic
Kaltenbach & Voigt GmbH, DE
EFA
Dec 8, 2016K161488ESTETICA Dental Treatment Unit and Accessories
Kaltenbach & Voigt GmbH, DE
EIA
Apr 9, 2015K143465MASTERmatic LUX
Kaltenbach & Voigt GmbH, DE
EFA
Aug 15, 2014K140308MASTERSURG / EXPERTSURG
Kaltenbach & Voigt GmbH, DE
EBW
Sep 27, 2013K130560MASTERTORQUE LUX 8900 L
Kaltenbach & Voigt GmbH, DE
EFB
Sep 24, 2013K123402DIAGNOCAM
Kaltenbach & Voigt GmbH, DE
NTK
Aug 19, 2011K103027ELECTROTORQUE TLC
Kaltenbach & Voigt GmbH
EBW
Nov 3, 2009K092446INTRA LUX HEAD 3 LDSY
Kaltenbach & Voigt GmbH & Co.
EFA
Jun 6, 2008K080677COMFORTRONIC 4894 AND COMFORTDRIVE 200XDA HANDPIECE
Kaltenbach & Voigt GmbH & Co.
EIA

Latest recalls

DateFirm and productCodeLinked 510(k)
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