锥形钛基托
K号: K243521 · 2025-05-01
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决定日期2025-05-01
产品代码NHA
咨询委员会DE
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器械摘要
Conical Ti Base abutments is the device name listed in this FDA 510(k) record. The listed applicant is BioHorizons Implant Systems, Inc.. It received FDA 510(k) clearance on 2025-05-01 under 510(k) number K243521. 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 Conical Ti Base abutments?
Conical Ti Base abutments is a medical device that received FDA 510(k) clearance on 2025-05-01. The listed applicant is BioHorizons Implant Systems, Inc.. The 510(k) number is K243521.
When did Conical Ti Base abutments receive FDA 510(k) clearance?
Conical Ti Base abutments received FDA 510(k) clearance on 2025-05-01, under 510(k) number K243521.
Who is the listed applicant for Conical Ti Base abutments?
The FDA 510(k) record lists BioHorizons Implant Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Conical Ti Base abutments?
The FDA product code for Conical Ti Base abutments is NHA.
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BioHorizons Implant Systems, 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。
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, LLCK253999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 ABK261147Neodent植入系统 - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC 兼容 Ti-BasesBioHorizons Implant Systems, Inc.
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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