Class Class II
Navident (K233563)
Description
Navident by Claronav, Inc., an FDA 510(k) cleared dental device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK233563
Clearance Date2024-07-25
Clearance TypeTraditional
Product CodePLV
Regulation Number872.4120
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K233563
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. Navident (K233563) cites 0 predicate devices and is itself cited by 1 later device.
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K253954 | X-Guide Surgical Navigation System | X-Nav Technologies, LLC | 2026 |
Trace the full predicate network for K233563
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.