ZENEX Implant System
K-Number: K211090 · 2022-04-13
Device Summary
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.
Related Clinical Trials
Related PubMed Literature
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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.