eXaSkin Plus
K号: K252784 · 2026-05-22
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器械摘要
eXaSkin Plus is the device name listed in this FDA 510(k) record. The listed applicant is Anatomical Geometry S.L.. It received FDA 510(k) clearance on 2026-05-22 under 510(k) number K252784. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the eXaSkin Plus?
eXaSkin Plus is a medical device that received FDA 510(k) clearance on 2026-05-22. The listed applicant is Anatomical Geometry S.L.. The 510(k) number is K252784.
When did eXaSkin Plus receive FDA 510(k) clearance?
eXaSkin Plus received FDA 510(k) clearance on 2026-05-22, under 510(k) number K252784.
Who is the listed applicant for eXaSkin Plus?
The FDA 510(k) record lists Anatomical Geometry S.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for eXaSkin Plus?
The FDA product code for eXaSkin Plus is MUJ.
相关临床试验
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相关器械（代码：MUJ）
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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