RODIN Palette Naturalizing Kit— 510(k) K223365

Name: FDA 510(k) clearance K223365
Creator: U.S. Food and Drug Administration
Published: 2023-03-27

Substantially Equivalent

Belport Company, Inc., Gingi-Pak

FDA 510(k) clearance K223365 for RODIN Palette Naturalizing Kit, Substantially Equivalent on 2023-03-27. Applicant: Belport Company, Inc., Gingi-Pak. Device class: 2.

Clearance details

Applicant: Belport Company, Inc., Gingi-Pak
Product code: Code EBD
Device class: Class 2
Regulation: 21 CFR 872.3310
Advisory panel: Dental
Date received: 2022-11-03
Decision date: 2023-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

Download summary PDF View on FDA.gov ↗

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