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FDA 510(k)

Monodek™(多迪氧烷)染綠紫色單絲合成可吸收外科縫線

K 號:K261988 · 2026-07-09

決定日期2026-07-09
產品代碼NEW
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical Suture is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical, LLC. It received FDA 510(k) clearance on 2026-07-09 under 510(k) number K261988. The device is classified under product code NEW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical Suture?

Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical Suture is a medical device that received FDA 510(k) clearance on 2026-07-09. The listed applicant is Teleflex Medical, LLC. The 510(k) number is K261988.

When did Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical Suture receive FDA 510(k) clearance?

Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical Suture received FDA 510(k) clearance on 2026-07-09, under 510(k) number K261988.

Who is the listed applicant for Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical Suture?

The FDA 510(k) record lists Teleflex Medical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical Suture?

The FDA product code for Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical Suture is NEW.

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。

其他以 Teleflex Medical, LLC 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。

相關器械(代碼:NEW)

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

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