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FDA 510(k)

ZENEX Implant System

K-Number: K211090 · 2022-04-13

Decision Date2022-04-13
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZENEX Implant System is a medical device manufactured by Izenimplant Co., Ltd.. It received FDA 510(k) clearance on 2022-04-13 under approval number K211090. 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 ZENEX Implant System?

ZENEX Implant System is a medical device that received FDA 510(k) clearance on 2022-04-13. It is manufactured by Izenimplant Co., Ltd.. The 510(k) number is K211090.

When was ZENEX Implant System approved by the FDA?

ZENEX Implant System received FDA 510(k) clearance on 2022-04-13, under approval number K211090.

What company makes ZENEX Implant System?

ZENEX Implant System is manufactured by Izenimplant Co., Ltd..

What is the FDA product code for ZENEX Implant System?

The FDA product code for ZENEX Implant System is DZE.

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Official Source

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