# K211854: VITA Akzent LC

- Pathway: 510(k) (Traditional)
- Applicant: Vita Zahnfabrik GmbH H Rauter & CO
- Decided: Nov 22, 2021 after 159 days
- Product code: EBD (Coating, Filling Material, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3310
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K123761 (2013). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123761: Vita Enamic Stains, Innovation Meditech GmbH (2013) Summary page 4.

## Most influential descendants
- 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

## Indications for use
VITA AKZENT LC Indication range: • Restorations made of hybrid ceramic • Restorations made of light-curing veneering material • Restorations made of CAD/CAM composites • Prefabricated Teeth • Denture bases

Source page: https://510kreport.com/device/K211854
Methodology: https://510kreport.com/methodology