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FDA 510(k)

ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments

K-Number: K253372 · 2026-05-14

ApplicantHiossen, Inc.
Decision Date2026-05-14
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Hiossen, Inc.. It received FDA 510(k) clearance on 2026-05-14 under 510(k) number K253372. 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 ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments?

ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments is a medical device that received FDA 510(k) clearance on 2026-05-14. The listed applicant is Hiossen, Inc.. The 510(k) number is K253372.

When did ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments receive FDA 510(k) clearance?

ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments received FDA 510(k) clearance on 2026-05-14, under 510(k) number K253372.

Who is the listed applicant for ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments?

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

What is the FDA product code for ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments?

The FDA product code for ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing Abutments is NHA.

Related Clinical Trials

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.

NCT07624331Volumetric Analysis of Peri-Implant Soft Tissue Changes Between Polyethereketone(PEEK) Anatomic Healing Abutments and Standard Healing Abutments in Posterior Single Implant RestorationsRECRUITING

Other records listing Hiossen, Inc. 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.

K251427EK MULTI ANGLED 30 ABUTMENTK241003HIOSSEN Pre-milled Abutment (ET Pre-milled Abutment & EK Pre-milled Abutment)K240232EK D3.3 and Ultra Wide ImplantsK233389EK Digital AbutmentsK222636ET Abutment SystemK203360EK Implants and Abutments 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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