# K132230: Ice Zirkon Transluzent

- Pathway: 510(k) (Traditional)
- Applicant: Zirkonzahn Srl
- Decided: Nov 5, 2014 after 475 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: 1 generation back to K061851 (2006). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061851: Zirkonzahn Ice, Zirkonzahn GmbH (2006) Summary page 4.

## Most influential descendants
- K151490: Prettau Anterior T0 (2015), 0 descendants of its own

## Indications for use
For the fabrication of metal free single and multiple unit crowns/bridges, inlays, onlays bonded dental restorations.

Source page: https://510kreport.com/device/K132230
Methodology: https://510kreport.com/methodology