Redermo 伤口基质
K号: K260020 · 2026-04-16
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器械摘要
Redermo Wound Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Kreate Medical Co., Ltd.. It received FDA 510(k) clearance on 2026-04-16 under 510(k) number K260020. The device is classified under product code QSZ. FDA Decision: Substantially Equivalent.
常见问题
What is the Redermo Wound Matrix?
Redermo Wound Matrix is a medical device that received FDA 510(k) clearance on 2026-04-16. The listed applicant is Beijing Kreate Medical Co., Ltd.. The 510(k) number is K260020.
When did Redermo Wound Matrix receive FDA 510(k) clearance?
Redermo Wound Matrix received FDA 510(k) clearance on 2026-04-16, under 510(k) number K260020.
Who is the listed applicant for Redermo Wound Matrix?
FDA 510(k)记录将北京科瑞特医疗科技有限公司列为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for Redermo Wound Matrix?
The FDA product code for Redermo Wound Matrix is QSZ.
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Beijing Kreate Medical Co., 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：QSZ）
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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