Class Class II
KnoxFog Anti-fogging Device (K251068)
Description
KnoxFog Anti-fogging Device by Uv One Hygienics, Inc., an FDA 510(k) cleared gastroenterology, urology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251068
Clearance Date2025-08-27
Clearance TypeTraditional
Product CodeOCT
Regulation Number876.1500
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251068
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. KnoxFog Anti-fogging Device (K251068) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K163257 | VitreOx Anti-fog Solution | Sio2 Nanotech, LLC | 2017 |
Trace the full predicate network for K251068
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.