DIAGNODENT 2190 WITH PERIODONTAL PROBE— 510(k) K060080

Name: FDA 510(k) clearance K060080
Creator: U.S. Food and Drug Administration
Published: 2006-02-08

Substantially Equivalent

Kavo Dental Corporation

FDA 510(k) clearance K060080 for DIAGNODENT 2190 WITH PERIODONTAL PROBE, Substantially Equivalent on 2006-02-08. Applicant: Kavo Dental Corporation. Device class: 2.

Clearance details

Applicant: Kavo Dental Corporation
Product code: Code NTK
Device class: Class 2
Regulation: 21 CFR 872.1745
Advisory panel: Dental
Date received: 2006-01-10
Decision date: 2006-02-08
Decision: Substantially Equivalent
Clearance type: Special
Location: Deer Field, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code NTK

view all

K261847 — iTero Lumina Pro2026-07-02
K250771 — Primescan 22025-08-29
K240573 — iTero Lumina Pro2024-08-16
K213482 — TIA Tip, Cariosity, Transillumination Accessory Tip2022-04-29
K193659 — iTero Element 5D2020-03-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.