# K120134: Ips E.Max Press Multi

- Pathway: 510(k) (Traditional)
- Applicant: Ivoclar Vivadent, AG
- Decided: Jun 25, 2012 after 160 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
No predicates in its family tree.
9 later devices descend from it; 5 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K161269: CELTRA Press (2016), 2 descendants of its own
- K141887: Obsidian Press (All Ceramic and Pom) (2014), 2 descendants of its own
- K162888: Cercon (2017), 1 descendant of its own
- K262239: Obsidian® Press Over Zirconia (2026), 0 descendants of its own
- K241557: Cercon® yo ML (2024), 0 descendants of its own

## Indications for use
IPS e.max Press and IPS emax Press Multi is an all-ceramic system for the creation of Occlusal veneers Thin Veneers Veneers Inlays Onlays Crowns in the anterior and posterior region 3-unit bridges in the anterior region 3-unit bridges in the premolar region up to the second premolar as the termiinal abutment Crown, splinted crown or 3 unit bridge up to the second premolar placed on top of an implant abutment.

Source page: https://510kreport.com/device/K120134
Methodology: https://510kreport.com/methodology