# K102450: Ionolux Pro

- Pathway: 510(k) (Special)
- Applicant: Voco GmbH
- Decided: Oct 8, 2010 after 42 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
lonolux Pro is intended for the following applications: - 1.Restorations class Ill and V, especially cervical fillings and root caries - 2. Fillings on deciduous teeth - 3. Small class I fillings - 4. Temporary fillings - 5. Core build-up - 6. Lining

Source page: https://510kreport.com/device/K102450
Methodology: https://510kreport.com/methodology