FDA 510(k)

Redermo 瘘傷組織

K 號：K260020 · 2026-04-16

決定日期2026-04-16

產品代碼QSZ

決定相當於

器材摘要

Redermo Wound Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Kreate Medical Co., Ltd.. It received FDA 510(k) clearance on 2026-04-16 under 510(k) number K260020. The device is classified under product code QSZ. FDA Decision: Substantially Equivalent.

常見問題

What is the Redermo Wound Matrix?

Redermo Wound Matrix is a medical device that received FDA 510(k) clearance on 2026-04-16. The listed applicant is Beijing Kreate Medical Co., Ltd.. The 510(k) number is K260020.

When did Redermo Wound Matrix receive FDA 510(k) clearance?

Redermo Wound Matrix received FDA 510(k) clearance on 2026-04-16, under 510(k) number K260020.

Who is the listed applicant for Redermo Wound Matrix?

FDA 510(k) 記錄將北京創科醫療有限公司列為申請人。這並不單獨確立設備製造商的身份。

What is the FDA product code for Redermo Wound Matrix?

The FDA product code for Redermo Wound Matrix is QSZ.

其他以 Beijing Kreate Medical Co., Ltd. 為申請人之記錄

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。

K261646Redermax® 抗菌傷口組織 K251582Redermax 抗菌傷口維網

相關器械（代碼：QSZ）

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

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