# K110580: Narrow Connection Straumann Anatomic Ips E.Max Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Straumann USA
- Decided: Aug 12, 2011 after 164 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: 7 generations back to K894844 (1990). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091701: Straumann Modified Dental Abutment, Institut Straumann AG (2009) Summary page 1.

## Indications for use
Abutments are used in connection with the prosthetic restoration of Straumann dental implants. Abutments are intended to be placed into dental implants to provide support for prosthetic reconstructions such as crowns and bridges. Anatomic IFS emax Abutments are indicated for screw-retained single-tooth restorations and cement-retained single tooth and bridge restorations.

Source page: https://510kreport.com/device/K110580
Methodology: https://510kreport.com/methodology