turbodent 触控
K 號：K251425 · 2025-05-09
廣告
器材摘要
turbodent touch is the device name listed in this FDA 510(k) record. The listed applicant is Mectron S.P.A.. It received FDA 510(k) clearance on 2025-05-09 under 510(k) number K251425. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the turbodent touch?
turbodent touch is a medical device that received FDA 510(k) clearance on 2025-05-09. The listed applicant is Mectron S.P.A.. The 510(k) number is K251425.
When did turbodent touch receive FDA 510(k) clearance?
turbodent touch received FDA 510(k) clearance on 2025-05-09, under 510(k) number K251425.
Who is the listed applicant for turbodent touch?
The FDA 510(k) record lists Mectron S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for turbodent touch?
The FDA product code for turbodent touch is KOJ.
相關臨床試驗
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。
其他以 Mectron S.P.A. 為申請人之記錄
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。
廣告