# K924422: Palabond

- Pathway: 510(k) (Traditional)
- Applicant: Heraeus Kulzer, Inc.
- Decided: Nov 4, 1992 after 64 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.
6 later devices descend from it; 1 cites it directly.
0 of 7 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
- K982007: Trubyte Denture Bond Denture Bonding Agent (1998), 5 descendants of its own
- K051707: Eclipse Bonding Agent (2005), 4 descendants of its own
- K231578: Lucitone Digital Print Denture System (2023), 2 descendants of its own
- K262300: Denture Base Resin V2 (2026), 0 descendants of its own
- K243336: Lucitone Digital Print Denture™ System (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K924422
Methodology: https://510kreport.com/methodology