A-Silicone 用于咬合登记
K号: K201684 · 2020-09-24
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器械摘要
常见问题
What is the A-Silicone for Bite Registration?
A-Silicone for Bite Registration is a medical device that received FDA 510(k) clearance on 2020-09-24. The listed applicant is Shandong Huge Dental Material Corporation. The 510(k) number is K201684.
When did A-Silicone for Bite Registration receive FDA 510(k) clearance?
A-Silicone for Bite Registration received FDA 510(k) clearance on 2020-09-24, under 510(k) number K201684.
Who is the listed applicant for A-Silicone for Bite Registration?
The FDA 510(k) record lists Shandong Huge Dental Material Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A-Silicone for Bite Registration?
The FDA product code for A-Silicone for Bite Registration is ELW.
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Shandong Huge Dental Material Corporation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：ELW）
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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