# K241557: Cercon® yo ML

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply Sirona
- Decided: Aug 28, 2024 after 89 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: 4 generations back to K060104 (2006). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K162888: Cercon, Dentsply Sirona (2017) Summary page 5.
- K161269: CELTRA Press, Dentsply Sirona (2016) Summary page 5.
- K112152: Cercon HT, Dentsply International, Inc. (2011) Summary page 5.

## Indications for use
Cercon® yo ML is indicated in the anterior and posterior segments for: - Crowns - Multi-unit bridges (with a maximum of two panties between abutment crowns) - Inlays, onlays and veneers

Source page: https://510kreport.com/device/K241557
Methodology: https://510kreport.com/methodology