# K262207: Cemented Plus Abutment

- Pathway: 510(k) (Traditional)
- Applicant: Unidental Co., Ltd.
- Decided: Sep 23, 2026 after 85 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: 18 generations back to K960026 (1996). 165 ancestors in all.
No later device cites it as a predicate yet.
0 of 166 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221315: UNIdental Symphony Implant System, Unidental Co., Ltd. (2023) Summary page 5.

## Indications for use
The Cemented Plus Abutment is indicated for use in partially or fully edentulous mandibles and maxillae, in support of prosthetic restorations including single crowns and fixed partial dentures.

Source page: https://510kreport.com/device/K262207
Methodology: https://510kreport.com/methodology