meddevicedb.com FDA Device Reference

TearCare System

K262479 Class II Special
Decision Date
2026-08-18
Sponsor / Applicant
Sight Sciences, Inc.

Technical Specification

510(k) Submission ID K262479
Product Code ORZ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.5200
Decision Date 2026-08-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TearCare System received FDA 510(k) clearance under submission number K262479, sponsored by Sight Sciences, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2026-08-18.

Classification & Regulation

This clearance is catalogued under FDA product code ORZ and 21 CFR 886.5200, within the Ophthalmic review panel as a Class II device.