FDA 510(k)

Ti-Base & 主修修复

K号: K240603 · 2024-06-05

决定日期2024-06-05

产品代码NHA

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决定实质等同

器械摘要

Ti-Base & Master Fix is the device name listed in this FDA 510(k) record. The listed applicant is Arum Dentistry Co., Ltd.. It received FDA 510(k) clearance on 2024-06-05 under 510(k) number K240603. 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 Ti-Base & Master Fix?

Ti-Base & Master Fix is a medical device that received FDA 510(k) clearance on 2024-06-05. The listed applicant is Arum Dentistry Co., Ltd.. The 510(k) number is K240603.

When did Ti-Base & Master Fix receive FDA 510(k) clearance?

Ti-Base & Master Fix received FDA 510(k) clearance on 2024-06-05, under 510(k) number K240603.

Who is the listed applicant for Ti-Base & Master Fix?

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

What is the FDA product code for Ti-Base & Master Fix?

The FDA product code for Ti-Base & Master Fix is NHA.

列明Arum Dentistry 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。

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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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