Smile Dx®
K 號：K242437 · 2025-05-14
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器材摘要
Smile Dx® is the device name listed in this FDA 510(k) record. The listed applicant is Cube Click, Inc.. It received FDA 510(k) clearance on 2025-05-14 under 510(k) number K242437. The device is classified under product code MYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Smile Dx®?
Smile Dx® is a medical device that received FDA 510(k) clearance on 2025-05-14. The listed applicant is Cube Click, Inc.. The 510(k) number is K242437.
When did Smile Dx® receive FDA 510(k) clearance?
Smile Dx® received FDA 510(k) clearance on 2025-05-14, under 510(k) number K242437.
Who is the listed applicant for Smile Dx®?
The FDA 510(k) record lists Cube Click, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Smile Dx®?
The FDA product code for Smile Dx® is MYN.
相關臨床試驗
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相關器械（代碼：MYN）
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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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