FDA applicant

Kavo Dental Corporation

Deer Field, IL2 decisions2006–20210 recalls

FDA records 2 decisions for Kavo Dental Corporation (Deer Field, IL) from 2006 to 2021: 2 510(k) clearances. Most are in product codes NTK (Light Transmission Caries Detector) and EGS (Handpiece, Contra- And Right-Angle Attachment…). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Kavo Dental GmbH”.

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

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Kavo Dental Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2007high 1 (2021) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Kavo Dental Corporation by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Kavo Dental Corporation’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Kavo”

FDA records each applicant name separately; these may or may not be the same firm.

Kavo America 24 Kavo DO Brasil Industria E Comercio Ltda 1 Kavo Dental Technologies, LLC 1

Kavo Dental Corporation

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Kavo”