Kaltenbach & Voigt GmbH - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Kaltenbach & Voigt GmbH has 9 FDA 510(k) cleared medical devices. Based in Orange, US.
Historical record: 9 cleared submissions from 2011 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Kaltenbach & Voigt GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Kaltenbach & Voigt GmbH
9 devices
Cleared
Nov 23, 2019
DEXIS CariVu 3-in-1 by KaVo
Dental
422d
Cleared
Apr 10, 2019
PROPHYflex 4
Dental
348d
Cleared
Mar 17, 2017
SMARTmatic
Dental
119d
Cleared
Dec 08, 2016
ESTETICA Dental Treatment Unit and Accessories
Dental
190d
Cleared
Apr 09, 2015
MASTERmatic LUX
Dental
126d
Cleared
Aug 15, 2014
MASTERSURG / EXPERTSURG
Dental
189d
Cleared
Sep 27, 2013
MASTERTORQUE LUX 8900 L
Dental
207d
Cleared
Sep 24, 2013
DIAGNOCAM
Dental
323d
Cleared
Aug 19, 2011
ELECTROTORQUE TLC
Dental
310d