橙彩CAD醫療設備基座
K 號：K253312 · 2025-12-23
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器材摘要
OrangeCAD Med Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Orangecad Med GmbH. It received FDA 510(k) clearance on 2025-12-23 under 510(k) number K253312. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the OrangeCAD Med Abutments?
OrangeCAD Med Abutments is a medical device that received FDA 510(k) clearance on 2025-12-23. The listed applicant is Orangecad Med GmbH. The 510(k) number is K253312.
When did OrangeCAD Med Abutments receive FDA 510(k) clearance?
OrangeCAD Med Abutments received FDA 510(k) clearance on 2025-12-23, under 510(k) number K253312.
Who is the listed applicant for OrangeCAD Med Abutments?
The FDA 510(k) record lists Orangecad Med GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OrangeCAD Med Abutments?
The FDA product code for OrangeCAD Med Abutments is NHA.
相關臨床試驗
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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。
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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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