# K222688: The Trust

- Pathway: 510(k) (Traditional)
- Applicant: Genoss Co., Ltd.
- Decided: Aug 9, 2024 after 703 days
- Product code: EKX (Handpiece, Direct Drive, Ac-Powered)
- Device class: 1
- Regulation: 21 CFR 872.4200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K003714 (2001). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180953: AnyCheck IMT-100, Dms Co., Ltd. (2019) Summary page 5.

## Indications for use
The Trust is indicated for use in measuring the stability of implants in the oral cavity and maxillofacial region. The Trust is restricted to usage with Dentium implant system, and the angle of the Attack Pole to the abutment must be maintained at 900 when in use.

Source page: https://510kreport.com/device/K222688
Methodology: https://510kreport.com/methodology