# K140877: Vericore Zirconia Blanks

- Pathway: 510(k) (Traditional)
- Applicant: Whip Mix Corp.
- Decided: Sep 3, 2014 after 149 days
- Product code: EIH (Powder, Porcelain)
- Device class: 2
- Regulation: 21 CFR 872.6660
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K073108 (2007). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092496: Copran ZR/Origin YZ, White Peaks Dental Systems GmbH & Co. KG (2009) Summary page 4.

## Most influential descendants
- K142670: Vericore Zirconia Blanks (2014), 1 descendant of its own
- K152443: Vericore Gradient Temporary Disc (2016), 0 descendants of its own

## Indications for use
Vericore zirconia blanks are made from pre-sintered zirconium dioxide intended to be used with CAD/CAM or manual milling machines. Vericore zirconia blanks are biocompatible and designed to fabricate; - Zirconia Substructures - Restorations (Including inlays, onlays, and veneers) - Crown Framework in the Anterior and Posterior regions - Bridge Framework in the Anterior and Posterior regions

Source page: https://510kreport.com/device/K140877
Methodology: https://510kreport.com/methodology