免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据，仅供一般参考，不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

Alexis® 照明伤口保护器-拉钩，刚性，中（CL402）；Alexis® 照明伤口保护器-拉钩，柔性，中（CL302）

K号: K253531 · 2026-02-23

申请人Applied Medical Resources Corporation
决定日期2026-02-23
产品代码KGW
咨询委员会SU 请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同

器械摘要

Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302) is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Resources Corporation. It received FDA 510(k) clearance on 2026-02-23 under 510(k) number K253531. The device is classified under product code KGW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302)?

Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302) is a medical device that received FDA 510(k) clearance on 2026-02-23. The listed applicant is Applied Medical Resources Corporation. The 510(k) number is K253531.

When did Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302) receive FDA 510(k) clearance?

Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302) received FDA 510(k) clearance on 2026-02-23, under 510(k) number K253531.

Who is the listed applicant for Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302)?

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

What is the FDA product code for Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302)?

The FDA product code for Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Retractor, Flexible, Medium (CL302) is KGW.

相关临床试验

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明Applied Medical Resources Corporation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。

K260982Alexis 照明伤口保护器-拉钩，柔性，特小（cl312）；Alexis 照明伤口保护器-拉钩，柔性，小（cl301）；Alexis 照明伤口保护器-拉钩，柔性，中（cl302）；Alexis 照明伤口保护器-拉钩，柔性，大（cl303）；Alexis 照明伤口保护器-拉钩，刚性，小（cl401）；Alexis 照明伤口保护器-拉钩，刚性，中（cl402）；Alexis 照明伤口保护器-拉钩，刚性，大（cl403）K252412Voyant® 电外科发生器（EA030/电外科发生器）K232880Inzii Ripstop 可重部署回收系统K222284Voyant Maryland融合设备（单步激活，EB212，EB213，EB214）K220969GelPOINT V-Path Vaginal Access SystemK211043Alexis 封闭式提取系统

查看所有 12 个设备 →

相关器械（代码：KGW）

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。

K260982Alexis 照明伤口保护器-拉钩，柔性，特小（cl312）；Alexis 照明伤口保护器-拉钩，柔性，小（cl301）；Alexis 照明伤口保护器-拉钩，柔性，中（cl302）；Alexis 照明伤口保护器-拉钩，柔性，大（cl303）；Alexis 照明伤口保护器-拉钩，刚性，小（cl401）；Alexis 照明伤口保护器-拉钩，刚性，中（cl402）；Alexis 照明伤口保护器-拉钩，刚性，大（cl403）Applied Medical Resources Corporation

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。

↑