FDA 510(k)

Carriere® 運動專業® 清晰咬合矯正器

K 號：K252760 · 2025-11-27

決定日期2025-11-27

產品代碼DYW

諮詢委員會DE

決定相當於

器材摘要

Carriere® Motion Pro® Clear Bite Corrector is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Organizers, Inc.. It received FDA 510(k) clearance on 2025-11-27 under 510(k) number K252760. The device is classified under product code DYW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Carriere® Motion Pro® Clear Bite Corrector?

Carriere® Motion Pro® Clear Bite Corrector is a medical device that received FDA 510(k) clearance on 2025-11-27. The listed applicant is Ortho Organizers, Inc.. The 510(k) number is K252760.

When did Carriere® Motion Pro® Clear Bite Corrector receive FDA 510(k) clearance?

Carriere® Motion Pro® Clear Bite Corrector received FDA 510(k) clearance on 2025-11-27, under 510(k) number K252760.

Who is the listed applicant for Carriere® Motion Pro® Clear Bite Corrector?

The FDA 510(k) record lists Ortho Organizers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Carriere® Motion Pro® Clear Bite Corrector?

The FDA product code for Carriere® Motion Pro® Clear Bite Corrector is DYW.

其他以 Ortho Organizers, Inc. 為申請人之記錄

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相關器械（代碼：DYW）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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