meddevicedb.com FDA Device Reference

HEXA100 (hexafocon A) Daily Wear Contact Lenses

K171077 Class II Traditional
Decision Date
2017-08-01
Sponsor / Applicant
Contamac, Ltd.

Technical Specification

510(k) Submission ID K171077
Product Code HQD
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5916
Decision Date 2017-08-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEXA100 (hexafocon A) Daily Wear Contact Lenses received FDA 510(k) clearance under submission number K171077, 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 2017-08-01.

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.