FDA applicant

Electronic Waveform Laboratory, Inc.

Huntington Beach, CA6 decisions1982–20110 recalls

FDA records 6 decisions for Electronic Waveform Laboratory, Inc. (Huntington Beach, CA) from 1982 to 2011: 6 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and LWM (Device, Electrical Dental Anesthesia). Its devices cite 3 predicates, 2 of them its own earlier devices. 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 Electronic Waveform Laboratory, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Electronic Waveform Laboratory, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Electronic”

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

Electronic Monitors, Inc. 3 Electronic Business Machine Co., Ltd. (Ebm) 3 Electronic Depilatory, Inc. 3 Electronic Diagnostics, Inc. 1 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 Waveform Laboratory, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Electronic”