# K060893: Modification to Rebilda DC

- Pathway: 510(k) (Special)
- Applicant: Voco GmbH
- Decided: May 25, 2006 after 52 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices 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.

## Most influential descendants
- K143104: Visalys Core, Visalys PL-Core, Visalys PL-Core-C, Visalys PL-Core-X (2015), 1 descendant of its own
- K191527: Visalys CemCore, Visalys Cem Core Try In Paste (2019), 0 descendants of its own

## Indications for use
Rebilda DC is intended for core build-up of vital and non-vital teeth

Source page: https://510kreport.com/device/K060893
Methodology: https://510kreport.com/methodology