Class Class II
Claritag Advanced (K222356)
Description
Claritag Advanced by Dgi Technologies, an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK222356
Clearance Date2023-05-18
Clearance TypeTraditional
Product CodeGEH
Regulation Number878.4350
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K222356
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. Claritag Advanced (K222356) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K211099 | Freeze’n Clear Skin Clinic Warts & Tags | Cryoconcepts LP | 2022 |
| K190747 | Claritag | Dgi Technologies | 2019 |
Trace the full predicate network for K222356
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.