# K070723: Futurabond DC/Single Dose

- Pathway: 510(k) (Traditional)
- Applicant: Voco GmbH
- Decided: Jun 7, 2007 after 84 days
- Product code: KLE (Agent, Tooth Bonding, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3200
- 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
Futurabond DC/Single Dose is intended for direct self- or dual curing composite restaurations and core build-ups, direct light-curing composite/compomer/ormocer-based restaurations, fixing root pins/posts with dual- or self-curing composite cements, indirect restaurations with the application of dual-curing/self-curing composite cements for bonding inlays, onlays, crowns and bridges.

Source page: https://510kreport.com/device/K070723
Methodology: https://510kreport.com/methodology