meddevicedb.com FDA Device Reference

Oxfore®100 (hexafocon A) Rigid Gas Permeable Contact Lenses

K221768 Class II Traditional
Decision Date
2023-05-05
Sponsor / Applicant
Paragon Vision Sciences, Inc.

Technical Specification

510(k) Submission ID K221768
Product Code HQD
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5916
Decision Date 2023-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Oxfore®100 (hexafocon A) Rigid Gas Permeable Contact Lenses received FDA 510(k) clearance under submission number K221768, sponsored by Paragon Vision Sciences, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2023-05-05.

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.