# K162888: Cercon

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply Sirona
- Decided: Feb 24, 2017 after 130 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). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 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.
- K161269: CELTRA Press, Dentsply Sirona (2016) Summary page 4.

## Most influential descendants
- K241557: Cercon® yo ML (2024), 0 descendants of its own

## Indications for use
Cercon® is indicated for all ceramic restorations for anterior and posterior locations, including crowns and 3-unit bridges in anterior and posterior regions.

Source page: https://510kreport.com/device/K162888
Methodology: https://510kreport.com/methodology