# K110589: Cimara

- Pathway: 510(k) (Traditional)
- Applicant: Voco GmbH
- Decided: May 27, 2011 after 86 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Cimara: Intraoral repairs of defects in ceramic or composite veneer, fixed, prosthetic work with metal frames. Cimara Zircon: Intraoral repairs of defects in ceramic veneer, fixed, all-ceramic restorations on zirconium oxide frames and other oxide ceramics Intraoral repairs of fractures on ceramic and composite inlays

Source page: https://510kreport.com/device/K110589
Methodology: https://510kreport.com/methodology