Class Class II
Onflex™ Mesh (K251955)
Description
Onflex™ Mesh by Davol Inc., Subsidiary of C. R. Bard, Inc., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251955
Clearance Date2025-07-24
Clearance TypeSpecial
Product CodeFTL
Regulation Number878.3300
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251955
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. Onflex™ Mesh (K251955) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K142711 | ONFLEX Mesh | C.R. Bard, Inc. | 2015 |
Trace the full predicate network for K251955
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.