FDA applicant

Electro Med Supply, Inc.

Penn Valley, CA8 decisions1986–19940 recalls

FDA records 8 decisions for Electro Med Supply, Inc. (Penn Valley, CA) from 1986 to 1994: 8 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Electro Med Supply, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Electro Med Supply, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Electro Med Supply, 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 “Electro”

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

Electro-Nucleonics Laboratories, Inc. 41 Electro-Catheter Corp. 35 Electro-Biology, Inc. 28 Electro Medical Systems SA 11 Electro-Nucleonics, Inc. 9 Electro Therapeutic Devices, Inc. 8 Electro-Med Health Industries, Inc. 6 Electro-Diagnostic Instruments 4 Electro Medical Systems (Ems Sa) 3 Electro Fiberoptics Corp. 3 Electro-Cap Intl., Inc. 3 Electro-Diagnostic Imaging, Inc. 2

Electro Med Supply, 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 “Electro”