# K874788: Ketac-Bond Aplicap

- Pathway: 510(k) (Traditional)
- Applicant: Espe GmbH (Us)
- Decided: Apr 12, 1988 after 141 days
- Product code: EMA (Cement, Dental)
- Device class: 2
- Regulation: 21 CFR 872.3275
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 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
- K960954: Ketac-Molar Aplicap (1996), 8 descendants of its own
- K994251: Ketac-Molar Quick (2000), 1 descendant of its own
- K992966: Reference (1999), 1 descendant of its own
- K123826: Vitro Molar (2013), 0 descendants of its own
- K101493: Advanced Glass Ionomer (K-130) Restorative (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K874788
Methodology: https://510kreport.com/methodology