Medentika 牙槽系統,Medentika CAD/CAM 牙槽,Medentika CAD/CAM TiBases,Medentika 多單元牙槽
K 號:K223113 · 2024-04-15
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器材摘要
常見問題
What is the Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments?
Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments is a medical device that received FDA 510(k) clearance on 2024-04-15. The listed applicant is Medentika GmbH. The 510(k) number is K223113.
When did Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments receive FDA 510(k) clearance?
Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments received FDA 510(k) clearance on 2024-04-15, under 510(k) number K223113.
Who is the listed applicant for Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments?
The FDA 510(k) record lists Medentika GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments?
The FDA product code for Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-unit Abutments is NHA.
相關臨床試驗
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其他以 Medentika GmbH 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。
相關器械(代碼:NHA)
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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