FDA 510(k)

Endoform 皮肤模板

K号: K260669 · 2026-06-24

决定日期2026-06-24

产品代码KGN

决定实质等同

器械摘要

Endoform Dermal Template is the device name listed in this FDA 510(k) record. The listed applicant is Aroa Biosurgery , Ltd.. It received FDA 510(k) clearance on 2026-06-24 under 510(k) number K260669. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

常见问题

What is the Endoform Dermal Template?

Endoform Dermal Template is a medical device that received FDA 510(k) clearance on 2026-06-24. The listed applicant is Aroa Biosurgery , Ltd.. The 510(k) number is K260669.

When did Endoform Dermal Template receive FDA 510(k) clearance?

Endoform Dermal Template received FDA 510(k) clearance on 2026-06-24, under 510(k) number K260669.

Who is the listed applicant for Endoform Dermal Template?

The FDA 510(k) record lists Aroa Biosurgery , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Endoform Dermal Template?

The FDA product code for Endoform Dermal Template is KGN.

列明Aroa Biosurgery , Ltd.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。

K250598Endoform 重建模板 - PLGA K231305Endoform 牙科膜 K223373Enivo™K200502Myriad Particles K200413Symphony K183398Endoform Restella

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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 K260596胶原蛋白伤口粉Ventris Medical K253521ECMT-100 WMDEcm Therapeutics, Inc.K253204CatalyzeBioTissue Holdings, Inc.K253974Roosin 胶原蛋白敷料Roosin Medical Co., Ltd.

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