FDA applicant

Contour Electrodes, Inc.

Herrin, IL4 decisions1987–19900 recalls

FDA records 4 decisions for Contour Electrodes, Inc. (Herrin, IL) from 1987 to 1990: 4 510(k) clearances. Most are in product codes DRX (Electrode, Electrocardiograph) and DRY (Monitor, Blood-Gas, On-Line, Cardiopulmonary…). 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 Contour Electrodes, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Contour Electrodes, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Contour Electrodes, 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 “Contour”

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

Contour Fabricators of Florida, Inc. 18 Contour Medical Technology, Inc. 9 Contour Fabricators, Inc. 8 Contour Research, LLC 2 Contour, Inc. 1 Contour Healer, LLC 1 Contour Medical Systems, Inc. 1 Contour Technology 1

Contour Electrodes, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Contour”