meddevicedb.com FDA Device Reference

P-CON (polymacon) Soft (hydrophilic) Contact Lenses (Tinted, Color)

K242855 Class II Traditional
Decision Date
2025-07-30
Sponsor / Applicant
E.O.S Co., Ltd.

Technical Specification

510(k) Submission ID K242855
Product Code LPL
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5925
Decision Date 2025-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

P-CON (polymacon) Soft (hydrophilic) Contact Lenses (Tinted, Color) received FDA 510(k) clearance under submission number K242855, sponsored by E.O.S 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 2025-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code LPL and 21 CFR 886.5925, within the Ophthalmic review panel as a Class II device.