# K192251: Livento Press, Soprano 10, Soprano

- Pathway: 510(k) (Traditional)
- Applicant: Cendres+Metaux SA
- Decided: Jan 15, 2020 after 148 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: 5 generations back to K024250 (2003). 12 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141400: Dcceram System, Ceramay GmbH & Co.Kg (2015) Summary page 4.

## Most influential descendants
- K251084: zirkon; structure; LFU shades, stains and glazes (2025), 0 descendants of its own

## Indications for use
The indications for use for Livento® press, Soprano® 10 and Soprano® are: -Veneers -Inlays and onlays -Partial crowns -Anterior and posterior tooth crowns -Hybrid abutment crown -3-pontic bridge in anterior tooth region -3-pontic bridge in the premolar region up to max. 2nd premolar as a permanent abutment

Source page: https://510kreport.com/device/K192251
Methodology: https://510kreport.com/methodology