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FDA 510(k)

SPI Dental Implant System

K-Number: K172240 · 2018-01-31

ApplicantMsi France
Decision Date2018-01-31
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SPI Dental Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Msi France. It received FDA 510(k) clearance on 2018-01-31 under 510(k) number K172240. 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 SPI Dental Implant System?

SPI Dental Implant System is a medical device that received FDA 510(k) clearance on 2018-01-31. The listed applicant is Msi France. The 510(k) number is K172240.

When did SPI Dental Implant System receive FDA 510(k) clearance?

SPI Dental Implant System received FDA 510(k) clearance on 2018-01-31, under 510(k) number K172240.

Who is the listed applicant for SPI Dental Implant System?

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

What is the FDA product code for SPI Dental Implant System?

The FDA product code for SPI Dental Implant System is DZE.

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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