Adin Short Implants
K号: K212775 · 2022-07-08
广告
决定日期2022-07-08
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
Adin Short Implants is the device name listed in this FDA 510(k) record. The listed applicant is Adin Dental Implants Systems , Ltd.. It received FDA 510(k) clearance on 2022-07-08 under 510(k) number K212775. 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 Adin Short Implants?
Adin Short Implants is a medical device that received FDA 510(k) clearance on 2022-07-08. The listed applicant is Adin Dental Implants Systems , Ltd.. The 510(k) number is K212775.
When did Adin Short Implants receive FDA 510(k) clearance?
Adin Short Implants received FDA 510(k) clearance on 2022-07-08, under 510(k) number K212775.
Who is the listed applicant for Adin Short Implants?
The FDA 510(k) record lists Adin Dental Implants Systems , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Adin Short Implants?
The FDA product code for Adin Short Implants is DZE.
相关临床试验
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。
列明Adin Dental Implants Systems , 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。
相关器械（代码：DZE）
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。
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。
广告