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FDA 510(k)

LOCATOR® Angled Abutment

K-Number: K250721 · 2025-08-20

ApplicantZest Anchors, LLC
Decision Date2025-08-20
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LOCATOR® Angled Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Zest Anchors, LLC. It received FDA 510(k) clearance on 2025-08-20 under 510(k) number K250721. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOCATOR® Angled Abutment?

LOCATOR® Angled Abutment is a medical device that received FDA 510(k) clearance on 2025-08-20. The listed applicant is Zest Anchors, LLC. The 510(k) number is K250721.

When did LOCATOR® Angled Abutment receive FDA 510(k) clearance?

LOCATOR® Angled Abutment received FDA 510(k) clearance on 2025-08-20, under 510(k) number K250721.

Who is the listed applicant for LOCATOR® Angled Abutment?

The FDA 510(k) record lists Zest Anchors, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOCATOR® Angled Abutment?

The FDA product code for LOCATOR® Angled Abutment is NHA.

Other records listing Zest Anchors, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260555LOCATOR® Angled AbutmentK252944LOCATOR® Angled AbutmentK243272LOCATOR Angled AbutmentK233587LOCATOR Angled Abutment (Various)K220252High Retention Attachment SystemK213391High Retention Attachment System

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Related Devices (Code: NHA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, Inc.K253922Neodent Scannable Healing AbutmentJJGC Indústria e Comércio de Materiais Dentários S.A.K254145Omni-Directional Multi-Unit Abutment System (Trade Name: Omnibut™)Smart Denture Conversions, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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