FDA 510(k)

BruxZir® 时尚 NOW

K号: K250223 · 2025-02-25

决定日期2025-02-25

产品代码EIH

咨询委员会DE 请注意，您没有提供具体的医疗设备监管文本内容，因此我无法进行翻译。请提供需要翻译的具体文本，我将根据您的要求进行翻译。

决定实质等同

器械摘要

BruxZir® Esthetic NOW is the device name listed in this FDA 510(k) record. The listed applicant is Prismatik Dentalcraft, Inc.. It received FDA 510(k) clearance on 2025-02-25 under 510(k) number K250223. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BruxZir® Esthetic NOW?

BruxZir® Esthetic NOW is a medical device that received FDA 510(k) clearance on 2025-02-25. The listed applicant is Prismatik Dentalcraft, Inc.. The 510(k) number is K250223.

When did BruxZir® Esthetic NOW receive FDA 510(k) clearance?

BruxZir® Esthetic NOW received FDA 510(k) clearance on 2025-02-25, under 510(k) number K250223.

Who is the listed applicant for BruxZir® Esthetic NOW?

FDA 510(k)记录将Prismatik Dentalcraft, Inc.列为申请人。这本身并不足以确立该设备的制造商。

What is the FDA product code for BruxZir® Esthetic NOW?

The FDA product code for BruxZir® Esthetic NOW is EIH.

列明Prismatik Dentalcraft, Inc.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。

K261802Glidewell™ 牙托树脂 K262239Obsidian® 压力压过氧化锆 K254283BruxZir® Shaded 16 PLUS K252582与Camlog® CONELOG® Implant System, Dentium® NR Line Implant Systems兼容的Inclusive®钛连接件 K252446BruxZir® NOW K250302柔性部分树脂

查看所有 37 个设备 →

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。