FDA 510(k)

MIS LYNX 锥形连接植入系统

K号: K241692 · 2024-11-25

决定日期2024-11-25

产品代码DZE

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决定实质等同

器械摘要

MIS LYNX Conical Connection Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Sirona, Inc.. It received FDA 510(k) clearance on 2024-11-25 under 510(k) number K241692. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MIS LYNX Conical Connection Implant System?

MIS LYNX Conical Connection Implant System is a medical device that received FDA 510(k) clearance on 2024-11-25. The listed applicant is Dentsply Sirona, Inc.. The 510(k) number is K241692.

When did MIS LYNX Conical Connection Implant System receive FDA 510(k) clearance?

MIS LYNX Conical Connection Implant System received FDA 510(k) clearance on 2024-11-25, under 510(k) number K241692.

Who is the listed applicant for MIS LYNX Conical Connection Implant System?

FDA 510(k)记录中列出Dentsply Sirona, Inc.为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for MIS LYNX Conical Connection Implant System?

The FDA product code for MIS LYNX Conical Connection Implant System is DZE.

列明Dentsply Sirona, Inc.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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