LANDR 接触镜盒
K号: K252175 · 2026-02-10
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决定日期2026-02-10
产品代码LRX
咨询委员会OP
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决定实质等同
器械摘要
LANDR Contact LENS Case is the device name listed in this FDA 510(k) record. The listed applicant is Fourth Axis, LLC. It received FDA 510(k) clearance on 2026-02-10 under 510(k) number K252175. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LANDR Contact LENS Case?
LANDR Contact LENS Case is a medical device that received FDA 510(k) clearance on 2026-02-10. The listed applicant is Fourth Axis, LLC. The 510(k) number is K252175.
When did LANDR Contact LENS Case receive FDA 510(k) clearance?
LANDR Contact LENS Case received FDA 510(k) clearance on 2026-02-10, under 510(k) number K252175.
Who is the listed applicant for LANDR Contact LENS Case?
The FDA 510(k) record lists Fourth Axis, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LANDR Contact LENS Case?
The FDA product code for LANDR Contact LENS Case is LRX.
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。
相关器械（代码：LRX）
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。
K250495MINI VP1 (PL67_F); MINI VP1 (PL61_F)Avizor S.A.K240095CAREUS 接触镜盒（型号 1，型号 2，型号 3，型号 4，型号 5，型号 6）Shanghai Care US Medical Product Co., Ltd.K231123Phoenix隐形眼镜盒 - 圆顶顶部扁平包装（CL-01）；Phoenix隐形眼镜盒 - 经典扁平包装（CL-02）；Phoenix隐形眼镜盒 - 太阳镜形状扁平包装（CL-03）Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.K173538Clear Care 清洁与消毒溶液，AOCup 镜盒带 AODiscAlcon Laboratories, Inc.K172925隐形眼镜盒，型号：A-1，B-1P L Overseas LimitedK173365Bausch + Lomb Boston 角膜塑形镜盒Bausch & Lomb, Incorporated
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。
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