510(k) Report

FDA applicant

Medical Illumination, Inc.

Arleta, CA10 decisions1992–19930 recalls

FDA records 10 decisions for Medical Illumination, Inc. (Arleta, CA) from 1992 to 1993: 10 510(k) clearances. Most are in product codes KZF (Device, Medical Examination, Ac Powered) and FSW (Light, Surgical, Endoscopic). 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 Medical Illumination, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Illumination, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medical Illumination, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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