FDA 510(k)

NizPlant 牙齿种植系统

K号: K250476 · 2025-12-23

决定日期2025-12-23

产品代码DZE

咨询委员会DE 请注意，您没有提供具体的医疗设备监管文本内容，因此我无法进行翻译。请提供需要翻译的具体文本，我将根据您的要求进行翻译。

决定实质等同

器械摘要

NizPlant Dental Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Paragon Implant Mfg., LLC. It received FDA 510(k) clearance on 2025-12-23 under 510(k) number K250476. 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 NizPlant Dental Implant System?

NizPlant Dental Implant System is a medical device that received FDA 510(k) clearance on 2025-12-23. The listed applicant is Paragon Implant Mfg., LLC. The 510(k) number is K250476.

When did NizPlant Dental Implant System receive FDA 510(k) clearance?

NizPlant Dental Implant System received FDA 510(k) clearance on 2025-12-23, under 510(k) number K250476.

Who is the listed applicant for NizPlant Dental Implant System?

FDA 510(k)记录中列出Paragon Implant Mfg., LLC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 NizPlant Dental Implant System?

The FDA product code for NizPlant Dental Implant System is DZE.

列明Paragon Implant Mfg., LLC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。

K261392TriActive 牙齿种植系统 K252145GEN5® 和 GEN5+® 3.3mmD 牙科种植体 K251756灭菌托盘 K251938GEN5 和 GEN5+ 牙科种植系统

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。