# K051535: Modification to:Registrado X-Tra

- Pathway: 510(k) (Special)
- Applicant: Voco GmbH
- Decided: Jun 28, 2005 after 18 days
- Product code: ELW (Material, Impression)
- Device class: 2
- Regulation: 21 CFR 872.3660
- 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
Registrado X-tra is suitable for bite registration. fixing of face bow registration and is a location material for intra-oral pin tracing template

Source page: https://510kreport.com/device/K051535
Methodology: https://510kreport.com/methodology