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FDA 510(k)

ATLANTIS Abutment for MIS Conical Connection Implants

K-Number: K193529 · 2020-03-05

ApplicantDentsply Sirona
Decision Date2020-03-05
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ATLANTIS Abutment for MIS Conical Connection Implants is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Sirona. It received FDA 510(k) clearance on 2020-03-05 under 510(k) number K193529. 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 ATLANTIS Abutment for MIS Conical Connection Implants?

ATLANTIS Abutment for MIS Conical Connection Implants is a medical device that received FDA 510(k) clearance on 2020-03-05. The listed applicant is Dentsply Sirona. The 510(k) number is K193529.

When did ATLANTIS Abutment for MIS Conical Connection Implants receive FDA 510(k) clearance?

ATLANTIS Abutment for MIS Conical Connection Implants received FDA 510(k) clearance on 2020-03-05, under 510(k) number K193529.

Who is the listed applicant for ATLANTIS Abutment for MIS Conical Connection Implants?

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

What is the FDA product code for ATLANTIS Abutment for MIS Conical Connection Implants?

The FDA product code for ATLANTIS Abutment for MIS Conical Connection Implants 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.

NCT05883202Effect of the Abutment-Prosthesis Connection on Marginal Bone Loss and Gingival Sealing Around Dental ImplantsSUSPENDEDNCT03528330Clinical, Radiological and Microbiological Outcomes of Implants With Two Different Connection Configurations, a Split-mouth RCT.COMPLETED

Other records listing Dentsply Sirona as applicant

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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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