FDA 510(k)

GenesisZr UHT700 氧化锆

K号: K201608 · 2021-01-28

决定日期2021-01-28

产品代码EIH

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

GenesisZr UHT700 Zirconia is the device name listed in this FDA 510(k) record. The listed applicant is United Dental Resources Corporation. It received FDA 510(k) clearance on 2021-01-28 under 510(k) number K201608. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the GenesisZr UHT700 Zirconia?

GenesisZr UHT700 Zirconia is a medical device that received FDA 510(k) clearance on 2021-01-28. The listed applicant is United Dental Resources Corporation. The 510(k) number is K201608.

When did GenesisZr UHT700 Zirconia receive FDA 510(k) clearance?

GenesisZr UHT700 Zirconia received FDA 510(k) clearance on 2021-01-28, under 510(k) number K201608.

Who is the listed applicant for GenesisZr UHT700 Zirconia?

The FDA 510(k) record lists United Dental Resources Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GenesisZr UHT700 Zirconia?

The FDA product code for GenesisZr UHT700 Zirconia is EIH.

列明United Dental Resources Corporation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。

K201915GenesisZr 4Y+ (ST1100) 氧化锆 K182642GenesisZr™ 4Y 氧化锆

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。