FDA 510(k)

Interojo 45（inofilcon A）软（亲水性）硅凝胶隐形眼镜，带GrabSoo Plus

K号: K260507 · 2026-05-29

决定日期2026-05-29

产品代码LPL

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决定实质等同

器械摘要

Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus is the device name listed in this FDA 510(k) record. The listed applicant is INTEROJO, Inc.. It received FDA 510(k) clearance on 2026-05-29 under 510(k) number K260507. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus?

Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus is a medical device that received FDA 510(k) clearance on 2026-05-29. The listed applicant is INTEROJO, Inc.. The 510(k) number is K260507.

When did Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus receive FDA 510(k) clearance?

Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus received FDA 510(k) clearance on 2026-05-29, under 510(k) number K260507.

Who is the listed applicant for Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus?

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

What is the FDA product code for Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus?

The FDA product code for Interojo 45 (inofilcon A) Soft (Hydrophilic) Silicone Hydrogel Contact Lens with GrabSoo Plus is LPL.

列明INTEROJO, Inc.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。

K221517POLYVUE (polymacon) 软性（亲水性）隐形眼镜，POLYVUE COLOR (polymacon) 软性（亲水性）隐形眼镜 K153766Clalen 54（hioxifilcon D）软（亲水）日戴隐形眼镜，Clalen 58（hioxifilcon A）软（亲水）日戴隐形眼镜

相关器械（代码：LPL）

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。

官方来源

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