FDA 510(k)

Straumann Variobase 基台 XC 用于桥/杆

K号: K253315 · 2026-01-22

决定日期2026-01-22

产品代码NHA

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决定实质等同

器械摘要

Straumann Variobase Abutments XC for Bridge/Bar is the device name listed in this FDA 510(k) record. The listed applicant is Institut Straumann AG. It received FDA 510(k) clearance on 2026-01-22 under 510(k) number K253315. 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 Straumann Variobase Abutments XC for Bridge/Bar?

Straumann Variobase Abutments XC for Bridge/Bar is a medical device that received FDA 510(k) clearance on 2026-01-22. The listed applicant is Institut Straumann AG. The 510(k) number is K253315.

When did Straumann Variobase Abutments XC for Bridge/Bar receive FDA 510(k) clearance?

Straumann Variobase Abutments XC for Bridge/Bar received FDA 510(k) clearance on 2026-01-22, under 510(k) number K253315.

Who is the listed applicant for Straumann Variobase Abutments XC for Bridge/Bar?

The FDA 510(k) record lists Institut Straumann AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Straumann Variobase Abutments XC for Bridge/Bar?

The FDA product code for Straumann Variobase Abutments XC for Bridge/Bar is NHA.

列明Institut Straumann AG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。

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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。

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