KnoxFog Anti-fogging Device— 510(k) K251068

Name: FDA 510(k) clearance K251068
Creator: U.S. Food and Drug Administration
Published: 2025-08-27

Substantially Equivalent

Uv One Hygienics, Inc.

FDA 510(k) clearance K251068 for KnoxFog Anti-fogging Device, Substantially Equivalent on 2025-08-27. Applicant: Uv One Hygienics, Inc.. Device class: 2.

Clearance details

Applicant: Uv One Hygienics, Inc.
Product code: Code OCT
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2025-04-07
Decision date: 2025-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mesa, AZ, US

Download summary PDF View on FDA.gov ↗

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