# K243272: LOCATOR Angled Abutment

- Pathway: 510(k) (Traditional)
- Applicant: Zest Anchors, LLC
- Decided: Jan 14, 2025 after 90 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: 16 generations back to K894595 (1990). 155 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 159 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K233587: LOCATOR Angled Abutment (Various), Zest Anchors, LLC (2024) Summary page 5.

## Most influential descendants
- K250721: LOCATOR® Angled Abutment (2025), 2 descendants of its own
- K252944: LOCATOR® Angled Abutment (2025), 1 descendant of its own
- K260555: LOCATOR® Angled Abutment (2026), 0 descendants of its own

## 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/K243272
Methodology: https://510kreport.com/methodology