Curajel™ 口腔膠
K 號：K260126 · 2026-06-15
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器材摘要
Curajel™ Oral Gel is the device name listed in this FDA 510(k) record. The listed applicant is USpharma, Ltd.. It received FDA 510(k) clearance on 2026-06-15 under 510(k) number K260126. The device is classified under product code OLR. FDA Decision: Substantially Equivalent.
常見問題
What is the Curajel™ Oral Gel?
Curajel™ Oral Gel is a medical device that received FDA 510(k) clearance on 2026-06-15. The listed applicant is USpharma, Ltd.. The 510(k) number is K260126.
When did Curajel™ Oral Gel receive FDA 510(k) clearance?
Curajel™ Oral Gel received FDA 510(k) clearance on 2026-06-15, under 510(k) number K260126.
Who is the listed applicant for Curajel™ Oral Gel?
The FDA 510(k) record lists USpharma, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Curajel™ Oral Gel?
The FDA product code for Curajel™ Oral Gel is OLR.
相關臨床試驗
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相關器械（代碼：OLR）
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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