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FDA 510(k)

UNIdental Symphony Implant System

K-Number: K221315 · 2023-10-25

Decision Date2023-10-25
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNIdental Symphony Implant System is a medical device manufactured by Unidental Co., Ltd.. It received FDA 510(k) clearance on 2023-10-25 under approval number K221315. 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 UNIdental Symphony Implant System?

UNIdental Symphony Implant System is a medical device that received FDA 510(k) clearance on 2023-10-25. It is manufactured by Unidental Co., Ltd.. The 510(k) number is K221315.

When was UNIdental Symphony Implant System approved by the FDA?

UNIdental Symphony Implant System received FDA 510(k) clearance on 2023-10-25, under approval number K221315.

What company makes UNIdental Symphony Implant System?

UNIdental Symphony Implant System is manufactured by Unidental Co., Ltd..

What is the FDA product code for UNIdental Symphony Implant System?

The FDA product code for UNIdental Symphony Implant System is DZE.

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Related PubMed Literature

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Official Source

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