ZENEX Implant System_Long
K-Number: K240560 · 2024-10-30
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.