FDA applicant

Sight Sciences, Inc.

Menlo Park, CA13 decisions2013–20260 recalls

FDA records 13 decisions for Sight Sciences, Inc. (Menlo Park, CA) from 2013 to 2026: 13 510(k) clearances. Most are in product codes MRH (Pump, Infusion, Ophthalmic) and ORZ (Eyelid Thermal Pulsation System). Its devices cite 14 predicates, 11 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Sight Sciences, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2013high 3 (2026) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Sight Sciences, Inc. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sight Sciences, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Sight”

FDA records each applicant name separately; these may or may not be the same firm.

Sight Diagnostics, Ltd. 1 Sight-N-Sound & Co. 1

Sight Sciences, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Sight”