虛擬對齊器Pro：虛擬對齊器FLX
K 號：K233356 · 2024-08-08
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器材摘要
Illusion Aligner Pro: Illusion Aligner FLX is the device name listed in this FDA 510(k) record. The listed applicant is Laxmi Dental Export Pvt., Ltd.. It received FDA 510(k) clearance on 2024-08-08 under 510(k) number K233356. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Illusion Aligner Pro: Illusion Aligner FLX?
Illusion Aligner Pro: Illusion Aligner FLX is a medical device that received FDA 510(k) clearance on 2024-08-08. The listed applicant is Laxmi Dental Export Pvt., Ltd.. The 510(k) number is K233356.
When did Illusion Aligner Pro: Illusion Aligner FLX receive FDA 510(k) clearance?
Illusion Aligner Pro: Illusion Aligner FLX received FDA 510(k) clearance on 2024-08-08, under 510(k) number K233356.
Who is the listed applicant for Illusion Aligner Pro: Illusion Aligner FLX?
The FDA 510(k) record lists Laxmi Dental Export Pvt., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Illusion Aligner Pro: Illusion Aligner FLX?
The FDA product code for Illusion Aligner Pro: Illusion Aligner FLX is NXC.
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。
相關器械（代碼：NXC）
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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