維登斯系列雷射
K 號：K252753 · 2026-01-24
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決定日期2026-01-24
產品代碼GEX
諮詢委員會SU
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決定相當於
器材摘要
Vydence Family of Lasers is the device name listed in this FDA 510(k) record. The listed applicant is Vydence Medical Industria E Commercio Ltda. It received FDA 510(k) clearance on 2026-01-24 under 510(k) number K252753. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常見問題
What is the Vydence Family of Lasers?
Vydence Family of Lasers is a medical device that received FDA 510(k) clearance on 2026-01-24. The listed applicant is Vydence Medical Industria E Commercio Ltda. The 510(k) number is K252753.
When did Vydence Family of Lasers receive FDA 510(k) clearance?
Vydence Family of Lasers received FDA 510(k) clearance on 2026-01-24, under 510(k) number K252753.
Who is the listed applicant for Vydence Family of Lasers?
The FDA 510(k) record lists Vydence Medical Industria E Commercio Ltda as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vydence Family of Lasers?
The FDA product code for Vydence Family of Lasers is GEX. This falls under the Gastroenterology category.
相關臨床試驗
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相關器械（代碼：GEX）
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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