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FDA 510(k)

MIS V3 Conical Connection Dental Implant System­

K-Number: K163349 · 2017-05-26

ApplicantMis Implants Technologies , Ltd.
Decision Date2017-05-26
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MIS V3 Conical Connection Dental Implant System­ is the device name listed in this FDA 510(k) record. The listed applicant is Mis Implants Technologies , Ltd.. It received FDA 510(k) clearance on 2017-05-26 under 510(k) number K163349. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIS V3 Conical Connection Dental Implant System­?

MIS V3 Conical Connection Dental Implant System­ is a medical device that received FDA 510(k) clearance on 2017-05-26. The listed applicant is Mis Implants Technologies , Ltd.. The 510(k) number is K163349.

When did MIS V3 Conical Connection Dental Implant System­ receive FDA 510(k) clearance?

MIS V3 Conical Connection Dental Implant System­ received FDA 510(k) clearance on 2017-05-26, under 510(k) number K163349.

Who is the listed applicant for MIS V3 Conical Connection Dental Implant System­?

The FDA 510(k) record lists Mis Implants Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIS V3 Conical Connection Dental Implant System­?

The FDA product code for MIS V3 Conical Connection Dental Implant System­ is DZE.

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.

NCT03528330Clinical, Radiological and Microbiological Outcomes of Implants With Two Different Connection Configurations, a Split-mouth RCT.COMPLETEDNCT05883202Effect of the Abutment-Prosthesis Connection on Marginal Bone Loss and Gingival Sealing Around Dental ImplantsSUSPENDEDNCT05122897Investigation of Biofilm Formation on Temporary push-on Rings of Implant CrownsRECRUITINGNCT05859113Evaluation of Marginal Bone Loss and Associated Factors Around Ziacom Dental Implants With Different Prosthetic ConnectionACTIVE_NOT_RECRUITINGNCT07557836Comparative Clinical Study of Implant Stability and Peri-implant Bone Loss in Two Implant DesignsCOMPLETED

Other records listing Mis Implants Technologies , Ltd. 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.

K182228MIS LOCKiT Abutments System, OT-Equators and Ball AttachmentsK180282MIS Internal Hex Dental Implant SystemK173326MIS CONNECT Conical Connection AbutmentK172505MIS C1 Narrow Platform Conical Connection Implant System, MIS C1 Wide Platform Conical Connection Abutments

Related Devices (Code: DZE)

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.

K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.K252731Promimic ZrP Surface Dental Implant; Promimic ZrP + HAnano Surface Dental ImplantPromimic ABK252031Adin Long Dental Implant SystemAdin Dental Implant Systems , Ltd.

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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