ARGEN PEARL BRAND ZIRCONIA— 510(k) K071410

Name: FDA 510(k) clearance K071410
Creator: U.S. Food and Drug Administration
Published: 2007-08-15

Substantially Equivalent

The Argen Corporation

FDA 510(k) clearance K071410 for ARGEN PEARL BRAND ZIRCONIA, Substantially Equivalent on 2007-08-15. Applicant: The Argen Corporation. Device class: 2.

Clearance details

Applicant: The Argen Corporation
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2007-05-21
Decision date: 2007-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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K260918 — Zolid Lunaris2026-06-29

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