meddevicedb.com FDA Device Reference

MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting Solution

K253795 Class II Traditional
Decision Date
2026-08-13
Sponsor / Applicant
Menicon Co, Ltd.

Technical Specification

510(k) Submission ID K253795
Product Code LPN
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5928
Decision Date 2026-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting Solution received FDA 510(k) clearance under submission number K253795, sponsored by Menicon Co, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2026-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code LPN and 21 CFR 886.5928, within the Ophthalmic review panel as a Class II device.