510(k) Report

510(k) · Cleared

Cleared

DEXIS CariVu 3-in-1 by KaVo

K182712510(k) TraditionalCleared Nov 23, 2019422-day reviewClass II21 CFR 872.1745

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Kaltenbach & Voigt GmbH · NTK Light Transmission Caries Detector

Cleared on Nov 23, 2019 as substantially equivalent to K123402 (Kaltenbach & Voigt GmbH, 2013) after a 422-day review. Its family tree reaches back 4 generations to 1994. 1 later device descends from it.

Decided
Nov 23, 2019
Review
422 days
Class
Class II
Product code
NTK
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K933455 (1994). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 1 other ancestor 1 generation forward: 1 descendant K123402 · Diagnocam · Kaltenbach & Voigt GmbH · 2013K043068 · Difoti Usb 2.0 System · Electro-Optical Sciences, Inc. · 2004K991098 · Difoti System · Electro-Optical Sciences, Inc. · 1999K933455 · Computed Oral Radiology System · Schick Technologies, Inc. · 19940
  1. Root · 4 generations backK933455 Computed Oral Radiology SystemSchick Technologies, Inc. · 1994
  2. 3 generations backK991098 Difoti SystemElectro-Optical Sciences, Inc. · 1999
  3. 2 generations backK043068 Difoti Usb 2.0 SystemElectro-Optical Sciences, Inc. · 2004
  4. 1 generation backK123402 DiagnocamKaltenbach & Voigt GmbH · 2013
  5. This deviceK182712 DEXIS CariVu 3-in-1 by KaVoKaltenbach & Voigt GmbH · 2019
  6. Descendant · cites it directly · 0 of its ownK250771 Primescan 2Dentsply Sirona, Inc. · 2025

Most influential descendants

Showing 1 of 1 · See all
  • K250771Primescan 2Dentsply Sirona, Inc. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K933455Computed Oral Radiology SystemSchick Technologies, Inc.1994—
−3K991098Difoti SystemElectro-Optical Sciences, Inc.1999—
−2K043068Difoti Usb 2.0 SystemElectro-Optical Sciences, Inc.2004—
−1K123402DiagnocamKaltenbach & Voigt GmbH2013—
0 (this device)K182712DEXIS CariVu 3-in-1 by KaVoKaltenbach & Voigt GmbH2019—
+1K250771Primescan 2Dentsply Sirona, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K182712, 1994–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in NTK? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new NTK device

  1. #1 K261847 iTero Lumina™ Proscore 13.4 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K123402Diagnocam
Summary page 4
…• Device Class: II • Product Code: NTK, NBL 3. Primary Predicate Device: o Proprietary Name: DIAGNOcam 2170 (K123402) o Manufacturer: Kaltenbach & Voigt GmbH o Common Name: Laser fluorescence caries de…
Kaltenbach & Voigt GmbH2013—
†K172007CamX Triton HD Proxi HeadDuerr Dental AG2017—
†K150672VistaCam iX ProofDurr Dental AG2016—

Also cleared against K123402: 1 other device →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K250771Primescan 2Dentsply Sirona, Inc.20250

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 25 years and passes through 3 companies; a new generation was cleared every 6.2 years on median.
  • None of the 6 ancestors has a recall.
  • Of its descendants, K250771 (Dentsply Sirona, Inc., 2025) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K123402.

How does its category compare?

All NTK devices

NTK Light Transmission Caries Detector: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · NTK

1in 2025

2007: 22013: 12017: 12019: 12020: 12022: 12024: 12025: 12026 (partial year): 1
2007high 2 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NTK

Too few NTK 510(k)s in any year since 2007 to give a median.

Recalls per year · NTK

No recall names NTK since 2007.

Adverse event reports per year · NTK

2in 2025

2017: 12023: 22025: 2
2007high 2 (2023) · low 0 (2007)2025

MAUDE reports naming product code NTK, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—00
20080—00
20090—00
20100—00
20110—00
20120—00
20131—00
20140—00
20150—00
20160—00
20171—01
20180—00
20191—00
20201—00
20210—00
20221—00
20230—02
20241—00
20251—02
20261—0—

What is it indicated for?

The DEXIS CariVu 3-in-1 by KaVo acquires patient images as a diagnostic aid for detection of smooth surface caries, occlusal caries, proximal caries, initial caries, secondary caries, and tooth cracks. The DEXIS Cari Vu 3-in-1 by KaVo is designed for use by a trained professional in the field of dentistry.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K182712: DEXIS CariVu 3-in-1 by KaVo.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K182712

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026