FDA applicant

Concord Imaging, Ltd.

Algonquin, IL1 decision1990–19900 recalls

FDA records 1 decision for Concord Imaging, Ltd. (Algonquin, IL) in 1990: 1 510(k) clearance. All are in product code JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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, radiology panel, where it files most

How often FDA has decided Concord Imaging, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Concord Imaging, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Concord”

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

Concord Laboratories, Inc. 42 Concord/Portex 23 Concord Medical Products 1 Concord Protex 1

Concord Imaging, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Concord”