# K143330: BruxZir Anterior

- Pathway: 510(k) (Special)
- Applicant: Prismatik Dentalcraft, Inc.
- Decided: Dec 15, 2014 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 K060104 (2006). 2 ancestors in all.
6 later devices descend from it; 4 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130924: Bruxzir Shaded, Prismatik Dentalcraft, Inc. (2013) Summary page 4.

## Most influential descendants
- K162888: Cercon (2017), 1 descendant of its own
- K161219: Zmaxx T Series (2017), 1 descendant of its own
- K250826: Multi M Series (2025), 0 descendants of its own
- K241557: Cercon® yo ML (2024), 0 descendants of its own
- K191902: Razor, Everest, U&C Liquid (2019), 0 descendants of its own

## Indications for use
The device is indicated for use by dental technicians in the construction of custom made all ceramic restorations for anterior and posterior location.

Source page: https://510kreport.com/device/K143330
Methodology: https://510kreport.com/methodology