# K131644: Ankylos Syncone Abutment 5(Degree)

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply International, Inc.
- Decided: Jan 22, 2014 after 231 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 K894595 (1990). 34 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041509: Ankylos Dental Implant System, Friadent GmbH (2004) Summary page 1.
- K122268: Angled Xive MP Abutment, Angled Ankylos, Dentsply International (2012) Summary page 1.

## Most influential descendants
- K151439: Atlantis Isus (2016), 0 descendants of its own

## Indications for use
SynCone® Abutments on osseointegrated Implants Anchorage of dentures retained by taper friction and supported by ANKYLOS® implants SynCone™ Abutments for immediate loading Immediate loading of an implant supported prosthesis in an edentulous mandible supported by 4 ANXYLOS® implants off at least 11 mm in length and placed interfaraminally.

Source page: https://510kreport.com/device/K131644
Methodology: https://510kreport.com/methodology