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FDA 510(k)

Eco Abutment, Multiunit Abutment

K-Number: K220253 · 2023-08-18

ApplicantDio Corporation
Decision Date2023-08-18
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Eco Abutment, Multiunit Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Dio Corporation. It received FDA 510(k) clearance on 2023-08-18 under 510(k) number K220253. 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 Eco Abutment, Multiunit Abutment?

Eco Abutment, Multiunit Abutment is a medical device that received FDA 510(k) clearance on 2023-08-18. The listed applicant is Dio Corporation. The 510(k) number is K220253.

When did Eco Abutment, Multiunit Abutment receive FDA 510(k) clearance?

Eco Abutment, Multiunit Abutment received FDA 510(k) clearance on 2023-08-18, under 510(k) number K220253.

Who is the listed applicant for Eco Abutment, Multiunit Abutment?

The FDA 510(k) record lists Dio Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Eco Abutment, Multiunit Abutment?

The FDA product code for Eco Abutment, Multiunit Abutment is NHA.

Other records listing Dio Corporation 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.

K210828DIOnavi-Denture02K193623DIOnavi-DentureK193404UF(II) Bar holder abutmentK192263UCLA CCM AbutmentK190048UF(II) Anatomic abutmentK181037DIO CAD/CAM Abutment

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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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