# K260555: LOCATOR® Angled Abutment

- Pathway: 510(k) (Special)
- Applicant: Zest Anchors, LLC
- Decided: Apr 9, 2026 after 50 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: 19 generations back to K894595 (1990). 158 ancestors in all.
No later device cites it as a predicate yet.
0 of 159 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K252944: LOCATOR® Angled Abutment, Zest Anchors, LLC (2025) Summary page 7.

## Indications for use
The LOCATOR Angled Abutment is indicated for the attachment of full or partial, fixed and removable, restorations retained by endosseous implants to restore masticatory function for the patient.

Source page: https://510kreport.com/device/K260555
Methodology: https://510kreport.com/methodology