FDA applicant

Energex Systems, Inc.

Washington, DC1 decision2005–20050 recalls

FDA records 1 decision for Energex Systems, Inc. (Washington, DC) in 2005: 1 510(k) clearance. All are in product code NHH (Device, Discharge, Electrostatic (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 Energex Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Energex Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Energex Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?