SurgiTwin
K号: K250290 · 2025-08-29
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器械摘要
SurgiTwin is the device name listed in this FDA 510(k) record. The listed applicant is Twinsight. It received FDA 510(k) clearance on 2025-08-29 under 510(k) number K250290. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SurgiTwin?
SurgiTwin is a medical device that received FDA 510(k) clearance on 2025-08-29. The listed applicant is Twinsight. The 510(k) number is K250290.
When did SurgiTwin receive FDA 510(k) clearance?
SurgiTwin received FDA 510(k) clearance on 2025-08-29, under 510(k) number K250290.
Who is the listed applicant for SurgiTwin?
The FDA 510(k) record lists Twinsight as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SurgiTwin?
The FDA product code for SurgiTwin is LLZ.
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相关器械（代码：LLZ）
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
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