DentMix VPS Impression Material— 510(k) K223892

Name: FDA 510(k) clearance K223892
Creator: U.S. Food and Drug Administration
Published: 2023-04-27

Substantially Equivalent

Innovative Product Brands, Inc.

FDA 510(k) clearance K223892 for DentMix VPS Impression Material, Substantially Equivalent on 2023-04-27. Applicant: Innovative Product Brands, Inc.. Device class: 2.

Clearance details

Applicant: Innovative Product Brands, Inc.
Product code: Code ELW
Device class: Class 2
Regulation: 21 CFR 872.3660
Advisory panel: Dental
Date received: 2022-12-28
Decision date: 2023-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Highland, CA, US

Download summary PDF View on FDA.gov ↗

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