FDA applicant

Medo U.S.A., Inc.

Wood Dale, IL2 decisions1984–19850 recalls

FDA records 2 decisions for Medo U.S.A., Inc. (Wood Dale, IL) from 1984 to 1985: 2 510(k) clearances. Most are in product codes JOW (Sleeve, Limb, Compressible) and ILJ (Bath, Hydro-Massage). 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, cardiovascular panel, where it files most

How often FDA has decided Medo U.S.A., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medo U.S.A., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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See the 510(k) Report

Other applicant names beginning “Medo”

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

Medo DX Pte., Ltd. 1 Medo.Ai 1

Medo U.S.A., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medo”