# K150919: ArgenZ Esthetic Plus

- Pathway: 510(k) (Abbreviated)
- Applicant: The Argen Corporation
- Decided: Jul 13, 2015 after 98 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: 3 generations back to K060104 (2006). 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)
- K143330: BruxZir Anterior, Prismatik Dentalcraft, Inc. (2014) Summary page 4.

## Indications for use
ArgenZ Esthetic Plus blanks are intended to be used in the fabrication of inlays, crowns, copings, and fixed bridges (up to 3 units) using various CAD/CAM systems.

Source page: https://510kreport.com/device/K150919
Methodology: https://510kreport.com/methodology