Adhese Universal DC, Cention Primer— 510(k) K210804

Name: FDA 510(k) clearance K210804
Creator: U.S. Food and Drug Administration
Published: 2022-06-07

Substantially Equivalent

Ivoclar Vivadent, AG

FDA 510(k) clearance K210804 for Adhese Universal DC, Cention Primer, Substantially Equivalent on 2022-06-07. Applicant: Ivoclar Vivadent, AG. Device class: 2.

Clearance details

Applicant: Ivoclar Vivadent, AG
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 2021-03-17
Decision date: 2022-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Schaan, LI

Download summary PDF View on FDA.gov ↗

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