# K961434: Vita Zeta Crown and Bridge Acrylic Veneering System

- Pathway: 510(k) (Traditional)
- Applicant: Vident
- Decided: Jul 8, 1996 after 84 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.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K152373: VITA VM LC Flow (2015), 3 descendants of its own
- K240660: Signum composite flow; Signum universal bond; Signum metal bond ; Signum composite; Signum matrix; Signum liquid; Signum cre-active (2024), 1 descendant of its own
- K251587: VITA VMLC Primer (2026), 0 descendants of its own
- K230644: Signum opaque F (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K961434
Methodology: https://510kreport.com/methodology