AquaVance Clear Fluoride Treatment— 510(k) K262775

Name: FDA 510(k) clearance K262775
Creator: U.S. Food and Drug Administration
Published: 2026-10-27

Substantially Equivalent

The Belport Company Inc., DBA Gingi-Pak

FDA 510(k) clearance K262775 for AquaVance Clear Fluoride Treatment, Substantially Equivalent on 2026-10-27. Applicant: The Belport Company Inc., DBA Gingi-Pak. Device class: 2.

Clearance details

Applicant: The Belport Company Inc., DBA Gingi-Pak
Product code: Product code LBH
Device class: Class 2
Regulation: 21 CFR 872.3260
Advisory panel: Dental
Date received: 2026-08-05
Decision date: 2026-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

Download summary PDF View on FDA.gov ↗

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K261404 — UltraEZ2026-04-30
K260830 — APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)2026-03-18

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