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FDA 510(k)

ZENEX Implant System_Long

K-Number: K240560 · 2024-10-30

Decision Date2024-10-30
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZENEX Implant System_Long is the device name listed in this FDA 510(k) record. The listed applicant is Izenimplant Co., Ltd.. It received FDA 510(k) clearance on 2024-10-30 under 510(k) number K240560. 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_Long?

ZENEX Implant System_Long is a medical device that received FDA 510(k) clearance on 2024-10-30. The listed applicant is Izenimplant Co., Ltd.. The 510(k) number is K240560.

When did ZENEX Implant System_Long receive FDA 510(k) clearance?

ZENEX Implant System_Long received FDA 510(k) clearance on 2024-10-30, under 510(k) number K240560.

Who is the listed applicant for ZENEX Implant System_Long?

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

What is the FDA product code for ZENEX Implant System_Long?

The FDA product code for ZENEX Implant System_Long is DZE.

Other records listing Izenimplant Co., Ltd. as applicant

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.

View all 8 devices →

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.

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.