# K160798: IPS e.max® Press Abutment Solutions for Viteo Base Ti

- Pathway: 510(k) (Abbreviated)
- Applicant: Ivoclar Vivadent, AG
- Decided: Dec 15, 2016 after 267 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- 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 K120053 (2012). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120053: Ips E.Max Press - Abutment Solutions, Ivoclar Vivadent, AG (2012) Summary page 5.

## Indications for use
IPS e.max Press Abutment Solutions for Viteo Base Ti is intended for use in partially or fully edentulous mandibles and maxillae in support of single or multi-unit cement retained restorations. IPS e.max Press Abutment Solutions is recommended for the fabrication of: - Hybrid abutments for single-tooth restorations - Hybrid abutment crowns for restorations IPS e.max Press Abutment Solutions for Viteo Base-Ti are compatible with the following Implant Systems Implant brand and type Clearance ID Platform and Implant Diameter(s) Bone Level® Straumann® Dental Implant System, K150938 NC: 3.3 mm RC: 4.1, 4.8 mm K130222 NobelActive® Nobel Biocare®, K071370 NP: 3.5 mm RP: 4.3, 5.0 mm K041661 Osseotite® Biomet 3i® Certain® BI-OC: 3.4 mm BI-OC: 4.1, 5.0 mm K111216 OsseoSpeed® Astra Tech AB K101732 OS: 3.5, 4.0 mm OS: 4.5, 5.0 mm K091239

Source page: https://510kreport.com/device/K160798
Methodology: https://510kreport.com/methodology