# K033221: Kavo Everest ZH-Blank

- Pathway: 510(k) (Special)
- Applicant: Kavo America Corporation
- Decided: Oct 28, 2003 after 25 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 K022996 (2002). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032081: Kavo Everest ZS-Blank Models, 42, 20, and 60, Kavo America (2003)
- K030607: Kavo Everest G-Blank, Kavo Everest G-Ceram, Coating Ceramic LF-3-PFM, Glaze and Colorings/Staining/Shades, Kavo America (2003)
- K022996: Vita in-Ceram YZ Cubes for Cerec, Vident (2002) Summary page 1.

## Indications for use
The KaVo Everest@ ZH-Blank is used in the manufacture of dental prosthetics.

Source page: https://510kreport.com/device/K033221
Methodology: https://510kreport.com/methodology