FDA 510(k)

胶原蛋白伤口粉

K号: K260596 · 2026-07-02

决定日期2026-07-02

产品代码KGN

决定实质等同

器械摘要

Collagen Wound Powder is the device name listed in this FDA 510(k) record. The listed applicant is Ventris Medical. It received FDA 510(k) clearance on 2026-07-02 under 510(k) number K260596. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

常见问题

What is the Collagen Wound Powder?

Collagen Wound Powder is a medical device that received FDA 510(k) clearance on 2026-07-02. The listed applicant is Ventris Medical. The 510(k) number is K260596.

When did Collagen Wound Powder receive FDA 510(k) clearance?

Collagen Wound Powder received FDA 510(k) clearance on 2026-07-02, under 510(k) number K260596.

Who is the listed applicant for Collagen Wound Powder?

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

What is the FDA product code for Collagen Wound Powder?

The FDA product code for Collagen Wound Powder is KGN.

列明Ventris Medical为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K250556多孔生物支架 K240765多孔生物支架 K240458合成骨泥 K221644合成骨泥

相关器械（代码：KGN）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K260652ColActive PlusCovalon Technologies, Ltd.K260711Accelagen Plus 手术基质，1cc（CG-01AP）；Accelagen Plus 手术基质，3cc（CG-03AP）；Accelagen Plus 手术基质，5cc（CG-05AP）；Accelagen Plus 手术条带，125x25x2mm（CG-125X25AP）；Accelagen Plus 手术条带，250x25x2mm（CG-250X25AP）Berkeley Advanced Biomaterials K260669Endoform 皮肤模板Aroa Biosurgery , Ltd.K253521ECMT-100 WMDEcm Therapeutics, Inc.K253204CatalyzeBioTissue Holdings, Inc.K253974Roosin 胶原蛋白敷料Roosin Medical Co., Ltd.

官方来源

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