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Sight Sciences, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories2
Latest FDA decision2026-08-04

SEC Filings: 1 filings on record. Latest: 8-K (2026-08-05). View on SEC EDGAR →

TypeNumberDevice NameCodeDateActions
510(k) K253760 OMNI Ultra Surgical System (1-110)MRH2026-08-04 View
510(k) K252409 TearCare MGX SystemORZ2026-04-27 View
510(k) K242786 TearCare MGX SystemORZ2025-04-15 View
510(k) K231084 TearCare MGX SystemORZ2023-12-27 View
510(k) K232214 OMNI Surgical SystemMRH2023-08-25 View
510(k) K213045 TearCare SystemORZ2021-12-21 View
510(k) K202678 OMNI Surgical SystemMRH2021-03-01 View
510(k) K201953 OMNI PLUS Surgical SystemMRH2020-08-11 View
510(k) K173332 OMNI Surgical SystemMRH2017-12-21 View
510(k) K171905 VISCO 360 Viscosurgical SystemMRH2017-07-27 View

Related Clinical Trials

NCT06948773A Study of the Helix Surgical System in Primary Open-Angle Glaucoma (POAG) and Cataract (HELIX)ACTIVE_NOT_RECRUITINGNCT07365735TearCare MGX™ System With and Without Warming HoldCOMPLETED
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