FDA 510(k)

IU植入系统牙根植入体

K号: K221969 · 2023-05-12

决定日期2023-05-12

产品代码NHA

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决定实质等同

器械摘要

IU Implant System Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Warantec Co., Ltd.. It received FDA 510(k) clearance on 2023-05-12 under 510(k) number K221969. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the IU Implant System Abutment?

IU Implant System Abutment is a medical device that received FDA 510(k) clearance on 2023-05-12. The listed applicant is Warantec Co., Ltd.. The 510(k) number is K221969.

When did IU Implant System Abutment receive FDA 510(k) clearance?

IU Implant System Abutment received FDA 510(k) clearance on 2023-05-12, under 510(k) number K221969.

Who is the listed applicant for IU Implant System Abutment?

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

What is the FDA product code for IU Implant System Abutment?

The FDA product code for IU Implant System Abutment is NHA.

列明Warantec Co., Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K221972Warantec 定制基台 K172345IU植入系统

相关器械（代码：NHA）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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官方来源

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