FDA applicant

The Lighthouse For the Blind, Inc.

Seattle, WA2 decisions1992–19940 recalls

FDA records 2 decisions for The Lighthouse For the Blind, Inc. (Seattle, WA) from 1992 to 1994: 2 510(k) clearances. Most are in product codes KZF (Device, Medical Examination, Ac Powered) and LYY (Latex Patient Examination Glove). 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 The Lighthouse For the Blind, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Lighthouse For the Blind, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Lighthouse For the Blind, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like The Lighthouse For the Blind, 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 “The”

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

Lighthouse Medical, Inc. 4 Lighthouse Technical Innovations, Inc. 1

The Lighthouse For the Blind, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”