FDA applicant

Arco Matic, Inc.

Mchenry, IL2 decisions1982–19820 recalls

FDA records 2 decisions for Arco Matic, Inc. (Mchenry, IL) in 1982: 2 510(k) clearances. All are in product code IQI (Orthosis, Limb Brace). 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 Arco Matic, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arco Matic, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Arco”

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

Arco Medical Products Co. 21 Arco Medic, Ltd. 1

Arco Matic, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Arco”