牙顿娜柔适夹板，优米勒美斯夹板，牙顿娜维瓦特姆，优米勒美斯夹板版本S
K号: K222604 · 2023-04-21
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器械摘要
常见问题
What is the dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S?
dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S is a medical device that received FDA 510(k) clearance on 2023-04-21. The listed applicant is Dentona AG. The 510(k) number is K222604.
When did dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S receive FDA 510(k) clearance?
dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S received FDA 510(k) clearance on 2023-04-21, under 510(k) number K222604.
Who is the listed applicant for dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S?
The FDA 510(k) record lists Dentona AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S?
The FDA product code for dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S is MQC.
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。
相关器械（代码：MQC）
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。
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