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FDA 510(k)

High Retention Attachment System

K-Number: K220252 · 2022-04-14

ApplicantZest Anchors, LLC
Decision Date2022-04-14
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

High Retention Attachment System 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 2022-04-14 under 510(k) number K220252. 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 High Retention Attachment System?

High Retention Attachment System is a medical device that received FDA 510(k) clearance on 2022-04-14. The listed applicant is Zest Anchors, LLC. The 510(k) number is K220252.

When did High Retention Attachment System receive FDA 510(k) clearance?

High Retention Attachment System received FDA 510(k) clearance on 2022-04-14, under 510(k) number K220252.

Who is the listed applicant for High Retention Attachment System?

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 High Retention Attachment System?

The FDA product code for High Retention Attachment System 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 AbutmentK250721LOCATOR® Angled AbutmentK243272LOCATOR Angled AbutmentK233587LOCATOR Angled Abutment (Various)K213391High 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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