Sight Sciences, Inc. - FDA 510(k) Cleared Devices

Sight Sciences, Inc. develops ophthalmic surgical devices, with a manufacturing facility in Laguna Beach, US. The company specializes in innovative solutions for eye surgery and tear film management.

The company has received 11 FDA 510(k) clearances from 11 total submissions since 2013. All submissions focus on ophthalmic devices. The latest clearance was granted in 2026, confirming active regulatory engagement and ongoing product development.

Sight Sciences' cleared portfolio includes surgical systems and viscosurgical products designed for anterior segment procedures. Notable cleared devices span tear care systems, multi-functional surgical platforms, and viscoelastic delivery systems. These products address key clinical needs in cataract surgery, glaucoma treatment, and dry eye management.

Explore the complete list of cleared device names, product codes, and clearance dates to learn more about Sight Sciences' regulatory history and product portfolio.

2 devices have linked clinical trials registered on ClinicalTrials.gov.