FDA 510(k)

Adin Customized Abutments

K号: K250178 · 2025-10-17

决定日期2025-10-17

产品代码NHA

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决定实质等同

器械摘要

Adin Customized Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Adin Dental Implant Systems , Ltd.. It received FDA 510(k) clearance on 2025-10-17 under 510(k) number K250178. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Adin Customized Abutments?

Adin Customized Abutments is a medical device that received FDA 510(k) clearance on 2025-10-17. The listed applicant is Adin Dental Implant Systems , Ltd.. The 510(k) number is K250178.

When did Adin Customized Abutments receive FDA 510(k) clearance?

Adin Customized Abutments received FDA 510(k) clearance on 2025-10-17, under 510(k) number K250178.

Who is the listed applicant for Adin Customized Abutments?

The FDA 510(k) record lists Adin Dental Implant Systems , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Adin Customized Abutments?

The FDA product code for Adin Customized Abutments is NHA.

列明Adin Dental Implant Systems , 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。

K252031Adin Long Dental Implant System K223714UniFit 牙齿种植系统

相关器械（代码：NHA）

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。

K262207水泥固定基台Unidental Co., Ltd.K260940BellaTek BarsZimVie US Corp, LLC K253999通用底座 ASC 启动；通用底座 ASC 非启动；通用底座 MUA ASC；临时基台启动和非启动；愈合基台锥形连接；Omnigrip 临床螺丝钛；Omnigrip 假体螺丝Nobel Biocare AB K261147Neodent植入系统 - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLC K260061BioHorizons CEREC 兼容 Ti-BasesBioHorizons Implant Systems, Inc.

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