# K140570: Chairside Attachment Processing Material

- Pathway: 510(k) (Traditional)
- Applicant: Zest Anchors, LLC
- Decided: Jun 16, 2014 after 102 days
- Product code: EBI (Resin, Denture, Relining, Repairing, Rebasing)
- Device class: 2
- Regulation: 21 CFR 872.3760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K011211 (2001). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110440: Quick UP, Voco GmbH (2011) Summary page 2.
- K021586: Secure Reline/Pickup Material, Imtec Corp. (2002) Summary page 2.
- K092912: Starfill 2B HV (High Viscosity) Rockcore, Model: 90838 and Starfill 2B LV (Low Viscosity), Model: 90150, Danville Materials, Inc. (2009) Summary page 2.
- K011211: Flowable Composite/ Ecuflow/ Luxaflow, Dmg USA, Inc. (2001) Summary page 2.

## Indications for use
Chairsidee Attachment Processing Material is a dual cure (either self or UV light) pink composite used to process attachments into dentures in a chairside or laboratory procedure.

Source page: https://510kreport.com/device/K140570
Methodology: https://510kreport.com/methodology