FDA applicant

Mt. Hood Mfr., Inc.

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Mt. Hood Mfr., Inc. (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code IOB (Lamp, Infrared, Non Heating). 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, physical medicine panel, where it files most

How often FDA has decided Mt. Hood Mfr., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mt. Hood Mfr., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mt. Hood Mfr., Inc.

Which product codes does it file in?

What has FDA decided for it lately?