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FDA 510(k)

MS Lide Implant Systems

K-Number: K181477 · 2020-10-20

ApplicantHangzhou Minsheng Lide Medical Science & Technology Co., Ltd.
Decision Date2020-10-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MS Lide Implant Systems is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-10-20 under 510(k) number K181477. 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 MS Lide Implant Systems?

MS Lide Implant Systems is a medical device that received FDA 510(k) clearance on 2020-10-20. The listed applicant is Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd.. The 510(k) number is K181477.

When did MS Lide Implant Systems receive FDA 510(k) clearance?

MS Lide Implant Systems received FDA 510(k) clearance on 2020-10-20, under 510(k) number K181477.

Who is the listed applicant for MS Lide Implant Systems?

The FDA 510(k) record lists Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MS Lide Implant Systems?

The FDA product code for MS Lide Implant Systems 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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