GeniPhys Collymer 自组装支架
K号: K250329 · 2025-06-25
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器械摘要
GeniPhys Collymer Self-Assembling Scaffold is the device name listed in this FDA 510(k) record. The listed applicant is Geniphys, Inc.. It received FDA 510(k) clearance on 2025-06-25 under 510(k) number K250329. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.
常见问题
What is the GeniPhys Collymer Self-Assembling Scaffold?
GeniPhys Collymer Self-Assembling Scaffold is a medical device that received FDA 510(k) clearance on 2025-06-25. The listed applicant is Geniphys, Inc.. The 510(k) number is K250329.
When did GeniPhys Collymer Self-Assembling Scaffold receive FDA 510(k) clearance?
GeniPhys Collymer Self-Assembling Scaffold received FDA 510(k) clearance on 2025-06-25, under 510(k) number K250329.
Who is the listed applicant for GeniPhys Collymer Self-Assembling Scaffold?
The FDA 510(k) record lists Geniphys, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GeniPhys Collymer Self-Assembling Scaffold?
The FDA product code for GeniPhys Collymer Self-Assembling Scaffold is KGN.
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：KGN）
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。
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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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