# K160436: CreoDent Solidex Custom Abutment

- Pathway: 510(k) (Traditional)
- Applicant: Creodent Prosthetics, Ltd.
- Decided: Sep 29, 2016 after 225 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: 11 generations back to K894595 (1990). 78 ancestors in all.
No later device cites it as a predicate yet.
0 of 79 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150012: CreoDent Solidex Customized Abutment, Creodent Prosthetics, Ltd. (2015) Summary page 6.

## Indications for use
The CreoDent Solidex® Customized Abutment is intended for use with an endosseous implant to support a prosthetic device in patients who are partially or completely endentulous. The device can be used for single or multiple-unit restorations. The prosthesis can be cemented or screw retained to the abutment. An abutment screw is used to secure the abutment to the endosseous implant. The CreoDent Solidex® Customized Abutment is compatible with the following: Astra Tech Osseospeed TX Implants 3.5mm, 4.5mm Hiossen TS Implants 3.5mm, 4.0mm

Source page: https://510kreport.com/device/K160436
Methodology: https://510kreport.com/methodology