# K230126: Dentis s-Clean Regular Abutment

- Pathway: 510(k) (Traditional)
- Applicant: Dentis Co., Ltd.
- Decided: Aug 4, 2023 after 199 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: 15 generations back to K894595 (1990). 153 ancestors in all.
No later device cites it as a predicate yet.
0 of 154 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171027: Dentis Dental Implant System, Dentis Co., Ltd. (2017) Summary page 4.
- K082843: Modificaton to: Dentis Dental Implant System, Dentis Co., Ltd. (2009) Summary page 4.
- K150344: Dentis Dental Implant System, Dentis Co., Ltd. (2015) Summary page 4.
- K210134: Dentis s-Clean s-Line, Dentis Co., Ltd. (2021) Summary page 4.
- K171694: s-Clean TiN Coating Abutments, Dentis Co., Ltd. (2017) Summary page 4.
- K161689: OSSTEM Implant System - Abutment, Osstem Implant Co., Ltd. (2017) Summary page 4.
- K210826: Healing Abutment, Cover Screw, Megagen Implant Co., Ltd. (2022) Summary page 4.

## Indications for use
Dentis s-Clean Regular Abutment is indicated for use in partially or fully edentulous mandibles and maxillae, in support of single or multiple unit restorations including; cemented retained, screw retained, or overdenture restorations, and terminal or intermediate abutment support for fixed bridgework. This system is dedicated for one and two stage surgical procedures. This system is intended for delayed loading.

Source page: https://510kreport.com/device/K230126
Methodology: https://510kreport.com/methodology