FDA applicant
East Texas Lighthouse For the Blind
FDA records 7 decisions for East Texas Lighthouse For the Blind (Tyler, TX) from 1985 to 1988: 7 510(k) clearances. Most are in product codes KME (Bedding, Disposable, Medical) and KKX (Drape, Surgical, Antimicrobial). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided East Texas Lighthouse For the Blind’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for East Texas Lighthouse For the Blind since 2007.
Recalls per year
No recall linked to its devices since 2007.
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