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FDA 510(k)

KnoxFog Anti-fogging Device

K-Number: K251068 · 2025-08-27

ApplicantUv One Hygienics, Inc.
Decision Date2025-08-27
Product CodeOCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KnoxFog Anti-fogging Device is a medical device manufactured by Uv One Hygienics, Inc.. It received FDA 510(k) clearance on 2025-08-27 under approval number K251068. The device is classified under product code OCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KnoxFog Anti-fogging Device?

KnoxFog Anti-fogging Device is a medical device that received FDA 510(k) clearance on 2025-08-27. It is manufactured by Uv One Hygienics, Inc.. The 510(k) number is K251068.

When was KnoxFog Anti-fogging Device approved by the FDA?

KnoxFog Anti-fogging Device received FDA 510(k) clearance on 2025-08-27, under approval number K251068.

What company makes KnoxFog Anti-fogging Device?

KnoxFog Anti-fogging Device is manufactured by Uv One Hygienics, Inc..

What is the FDA product code for KnoxFog Anti-fogging Device?

The FDA product code for KnoxFog Anti-fogging Device is OCT.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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