# K790589: Denture-Tight

- Pathway: 510(k) (Traditional)
- Applicant: Den-Mat Corp.
- Decided: Aug 10, 1979 after 136 days
- Product code: EBP (Reliner, Denture, Over The Counter)
- Device class: 2
- Regulation: 21 CFR 872.3560
- 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; 1 cites 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
- K101771: Reline-IT Model Reline-IT (2010), 1 descendant of its own
- K121318: Prosoft (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K790589
Methodology: https://510kreport.com/methodology