Dentalis Bio Solution Implants
K号: K161281 · 2017-01-11
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决定日期2017-01-11
产品代码DZE
咨询委员会DE
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器械摘要
Dentalis Bio Solution Implants is the device name listed in this FDA 510(k) record. The listed applicant is Dentalis Bio Solution Implants, LLC. It received FDA 510(k) clearance on 2017-01-11 under 510(k) number K161281. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Dentalis Bio Solution Implants?
Dentalis Bio Solution Implants is a medical device that received FDA 510(k) clearance on 2017-01-11. The listed applicant is Dentalis Bio Solution Implants, LLC. The 510(k) number is K161281.
When did Dentalis Bio Solution Implants receive FDA 510(k) clearance?
Dentalis Bio Solution Implants received FDA 510(k) clearance on 2017-01-11, under 510(k) number K161281.
Who is the listed applicant for Dentalis Bio Solution Implants?
The FDA 510(k) record lists Dentalis Bio Solution Implants, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dentalis Bio Solution Implants?
The FDA product code for Dentalis Bio Solution Implants is DZE.
相关临床试验
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相关器械（代码：DZE）
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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