Sight Sciences, Inc.
Sight Sciences, Inc. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2026, with 1 FDA device recall on record.
Top product codes for Sight Sciences, Inc.
FDA recalls by Sight Sciences, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Sight Sciences, Inc.
- K262479 — TearCare System
- K253760 — OMNI Ultra Surgical System (1-110)
- K252409 — TearCare MGX System
- K242786 — TearCare MGX System
- K231084 — TearCare MGX System
- K232214 — OMNI Surgical System
- K213045 — TearCare System
- K202678 — OMNI Surgical System
- K201953 — OMNI PLUS Surgical System
- K173332 — OMNI Surgical System
- K171905 — VISCO 360 Viscosurgical System
- K143205 — Viscoelastic Injector
- K132494 — VISCOELASTIC INJECTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.