LuxaPrint 正畸增强型
K号: K210940 · 2021-09-03
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器械摘要
LuxaPrint Ortho Plus is the device name listed in this FDA 510(k) record. The listed applicant is Dmg Digital Enterprises SE. It received FDA 510(k) clearance on 2021-09-03 under 510(k) number K210940. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.
常见问题
What is the LuxaPrint Ortho Plus?
LuxaPrint Ortho Plus is a medical device that received FDA 510(k) clearance on 2021-09-03. The listed applicant is Dmg Digital Enterprises SE. The 510(k) number is K210940.
When did LuxaPrint Ortho Plus receive FDA 510(k) clearance?
LuxaPrint Ortho Plus received FDA 510(k) clearance on 2021-09-03, under 510(k) number K210940.
Who is the listed applicant for LuxaPrint Ortho Plus?
The FDA 510(k) record lists Dmg Digital Enterprises SE as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LuxaPrint Ortho Plus?
The FDA product code for LuxaPrint Ortho Plus 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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