Sight Sciences, Inc.

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
10
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1001-2022Class IITearCare version 1.0 SmartHubsMarch 23, 2022

Recent 510(k) Clearances

K-NumberDeviceDate
K242786TearCare MGX SystemApril 15, 2025
K231084TearCare MGX SystemDecember 27, 2023
K232214OMNI Surgical SystemAugust 25, 2023
K213045TearCare SystemDecember 21, 2021
K202678OMNI Surgical SystemMarch 1, 2021
K201953OMNI PLUS Surgical SystemAugust 11, 2020
K173332OMNI Surgical SystemDecember 21, 2017
K171905VISCO 360 Viscosurgical SystemJuly 27, 2017
K143205Viscoelastic InjectorDecember 5, 2014
K132494VISCOELASTIC INJECTOROctober 22, 2013