MASTERmatic LUX

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K143465 ↗

FDA Product Code

EFA

Device Class

Class I

Regulation

21 CFR Part 872.4200

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Mastertorque Lux 8900 L

  Class I

  FDA 510(k) K130560 Active Cleared 27 Sep 2013

• ESTETICA Dental Treatment Unit and Accessories

  Class I

  FDA 510(k) K161488 Active Cleared 8 Dec 2016

• SMARTmatic

  Class I

  FDA 510(k) K163239 Active Cleared 17 Mar 2017

• Mastersurg / Expertsurg

  Class I

  FDA 510(k) K140308 Active Cleared 15 Aug 2014

• PROPHYflex 4

  Class I

  FDA 510(k) K181110 Active Cleared 10 Apr 2019

• DEXIS CariVu 3-in-1 by KaVo

  Class II

  FDA 510(k) K182712 Active Cleared 23 Nov 2019

See all devices from Kaltenbach & Voigt GmbH →