# K913040: Ribbond (TM)

- Pathway: 510(k) (Traditional)
- Applicant: Ribbond, Inc.
- Decided: Oct 7, 1991 after 90 days
- Product code: EBI (Resin, Denture, Relining, Repairing, Rebasing)
- Device class: 2
- Regulation: 21 CFR 872.3760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 5 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K013881: Ribbond - Triaxial (2002), 2 descendants of its own
- K030820: Everstick Post (2003), 1 descendant of its own
- K063170: Tender Fiber (2007), 0 descendants of its own
- K061735: Infibra, Model 1200 (2006), 0 descendants of its own
- K060075: Fiber-Metal Post (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K913040
Methodology: https://510kreport.com/methodology