FDA applicant

Alimed, Inc.

Mchenry, IL11 decisions1979–19960 recalls

FDA records 11 decisions for Alimed, Inc. (Mchenry, IL) from 1979 to 1996: 11 510(k) clearances. Most are in product codes FMQ (Restraint, Protective) and KNP (Orthosis, Corrective Shoe). 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 Alimed, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alimed, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Alimed, Inc.

Which product codes does it file in?

What has FDA decided for it lately?