FDA 510(k)

QRS Dental Implants System

K-Number: K221910 · 2022-12-14

Decision Date2022-12-14

Product CodeDZE

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

QRS Dental Implants System is the device name listed in this FDA 510(k) record. The listed applicant is Qrs Medical , Ltd.. It received FDA 510(k) clearance on 2022-12-14 under 510(k) number K221910. 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 QRS Dental Implants System?

QRS Dental Implants System is a medical device that received FDA 510(k) clearance on 2022-12-14. The listed applicant is Qrs Medical , Ltd.. The 510(k) number is K221910.

When did QRS Dental Implants System receive FDA 510(k) clearance?

QRS Dental Implants System received FDA 510(k) clearance on 2022-12-14, under 510(k) number K221910.

Who is the listed applicant for QRS Dental Implants System?

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

What is the FDA product code for QRS Dental Implants System?

The FDA product code for QRS Dental Implants 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 AB K252031Adin 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.