# K790439: Contact Resin

- Pathway: 510(k) (Traditional)
- Applicant: Vivadent (Usa), Inc.
- Decided: Apr 10, 1979 after 34 days
- Product code: EBF (Material, Tooth Shade, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K092231: Gebdi Tribos 501 (2009), 0 descendants of its own
- K052779: Brecomp (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K790439
Methodology: https://510kreport.com/methodology