Neodent植牙系統 – 適用基座
K 號:K233857 · 2024-05-02
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器材摘要
常見問題
What is the Neodent Implant System – Custom Abutments?
Neodent Implant System – Custom Abutments is a medical device that received FDA 510(k) clearance on 2024-05-02. The listed applicant is JJGC Indústria e Comércio de Materiais Dentários S.A.. The 510(k) number is K233857.
When did Neodent Implant System – Custom Abutments receive FDA 510(k) clearance?
Neodent Implant System – Custom Abutments received FDA 510(k) clearance on 2024-05-02, under 510(k) number K233857.
Who is the listed applicant for Neodent Implant System – Custom Abutments?
The FDA 510(k) record lists JJGC Indústria e Comércio de Materiais Dentários S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Neodent Implant System – Custom Abutments?
The FDA product code for Neodent Implant System – Custom Abutments is NHA.
相關臨床試驗
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其他以 JJGC Indústria e Comércio de Materiais Dentários S.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。
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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