510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K182712Substantially Equivalent

DEXIS CariVu 3-in-1 by KaVo

Kaltenbach & Voigt GmbH, Biberach, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K182712 is the FDA 510(k) clearance record for DEXIS CariVu 3-in-1 by KaVo, a class II device, cleared for Kaltenbach & Voigt GmbH on under FDA product code NTK (Light Transmission Caries Detector). FDA records list 11 510(k) clearances for Kaltenbach & Voigt GmbH, from to . As of , FDA records show no recalls naming K182712.

Clearance record

Decision date
Received
(422 days to decision)
Product code
NTK Light Transmission Caries Detector
Regulation
21 CFR 872.1745
Device class
Class II
Review panel
Dental
Applicant
Kaltenbach & Voigt GmbH Bismarckring 39, Biberach, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NTK

Trailing 12 months
1 clearance under product code NTK in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code NTK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260