meddevicedb.com FDA Device Reference

Optimum Infinite (tisilfocon A) Daily Wear Contact Lenses

K212631 Class II Traditional
Decision Date
2022-03-17
Sponsor / Applicant
Contamac, Ltd.

Technical Specification

510(k) Submission ID K212631
Product Code HQD
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5916
Decision Date 2022-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Optimum Infinite (tisilfocon A) Daily Wear Contact Lenses received FDA 510(k) clearance under submission number K212631, sponsored by Contamac, 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 2022-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code HQD and 21 CFR 886.5916, within the Ophthalmic review panel as a Class II device.