牙齒植體單位
K 號：K242646 · 2025-04-11
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器材摘要
Dental Implant Unit is the device name listed in this FDA 510(k) record. The listed applicant is Guilin Aesthedent Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2025-04-11 under 510(k) number K242646. The device is classified under product code EBW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Dental Implant Unit?
Dental Implant Unit is a medical device that received FDA 510(k) clearance on 2025-04-11. The listed applicant is Guilin Aesthedent Medical Instruments Co., Ltd.. The 510(k) number is K242646.
When did Dental Implant Unit receive FDA 510(k) clearance?
Dental Implant Unit received FDA 510(k) clearance on 2025-04-11, under 510(k) number K242646.
Who is the listed applicant for Dental Implant Unit?
The FDA 510(k) record lists Guilin Aesthedent Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dental Implant Unit?
The FDA product code for Dental Implant Unit is EBW.
相關臨床試驗
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相關器械（代碼：EBW）
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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