FDA 510(k)

Bifix Veneer LC, Bifix Veneer 尝試用

K 號：K252606 · 2026-03-20

決定日期2026-03-20

產品代碼EMA

諮詢委員會DE

決定相當於

器材摘要

Bifix Veneer LC, Bifix Veneer Try-In is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2026-03-20 under 510(k) number K252606. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Bifix Veneer LC, Bifix Veneer Try-In?

Bifix Veneer LC, Bifix Veneer Try-In is a medical device that received FDA 510(k) clearance on 2026-03-20. The listed applicant is Voco GmbH. The 510(k) number is K252606.

When did Bifix Veneer LC, Bifix Veneer Try-In receive FDA 510(k) clearance?

Bifix Veneer LC, Bifix Veneer Try-In received FDA 510(k) clearance on 2026-03-20, under 510(k) number K252606.

Who is the listed applicant for Bifix Veneer LC, Bifix Veneer Try-In?

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

What is the FDA product code for Bifix Veneer LC, Bifix Veneer Try-In?

The FDA product code for Bifix Veneer LC, Bifix Veneer Try-In is EMA.

其他以 Voco GmbH 為申請人之記錄

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官方來源

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