FDA applicant

Electronic Diagnostics, Inc.

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for Electronic Diagnostics, Inc. (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code GZB (Stimulator, Spinal-Cord, Implanted (Pain Relief)). 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, neurology panel, where it files most

How often FDA has decided Electronic Diagnostics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Electronic Diagnostics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Electronic Diagnostics, 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 “Electronic”

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

Electronic Waveform Laboratory, Inc. 6 Electronic Monitors, Inc. 3 Electronic Business Machine Co., Ltd. (Ebm) 3 Electronic Depilatory, Inc. 3 Electronic Medical Sciences, Inc. 1 Electronic Control Concepts 1 Electronic Waveform Lab, Inc. 1 Electronic Health Technologies, Inc. 1 Electronic Energy, Inc. 1 Electronic Monitoring Devices, Inc. 1

Electronic Diagnostics, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Electronic”