FDA 510(k)

Alpha Endo手柄（Alpha Endo）

K号: K252223 · 2025-10-16

申请人SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.

决定日期2025-10-16

产品代码EKX

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决定实质等同

器械摘要

Alpha Endo Handpiece (Alpha Endo) is the device name listed in this FDA 510(k) record. The listed applicant is SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.. It received FDA 510(k) clearance on 2025-10-16 under 510(k) number K252223. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Alpha Endo Handpiece (Alpha Endo)?

Alpha Endo Handpiece (Alpha Endo) is a medical device that received FDA 510(k) clearance on 2025-10-16. The listed applicant is SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.. The 510(k) number is K252223.

When did Alpha Endo Handpiece (Alpha Endo) receive FDA 510(k) clearance?

Alpha Endo Handpiece (Alpha Endo) received FDA 510(k) clearance on 2025-10-16, under 510(k) number K252223.

Who is the listed applicant for Alpha Endo Handpiece (Alpha Endo)?

The FDA 510(k) record lists SHENZHEN SUPERLINE TECHNOLOGY CO., LTD. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Alpha Endo Handpiece (Alpha Endo)?

The FDA product code for Alpha Endo Handpiece (Alpha Endo) is EKX.

列明SHENZHEN SUPERLINE TECHNOLOGY 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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