KnoxFog Anti-fogging Device
K-Number: K251068 · 2025-08-27
Device Summary
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. The listed applicant is Uv One Hygienics, Inc.. The 510(k) number is K251068.
When did KnoxFog Anti-fogging Device receive FDA 510(k) clearance?
KnoxFog Anti-fogging Device received FDA 510(k) clearance on 2025-08-27, under 510(k) number K251068.
Who is the listed applicant for KnoxFog Anti-fogging Device?
The FDA 510(k) record lists Uv One Hygienics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KnoxFog Anti-fogging Device?
The FDA product code for KnoxFog Anti-fogging Device is OCT.
Related Devices (Code: OCT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.