FDA applicant

Matrix Electromedical, Inc.

Las Vegas, NV2 decisions1993–19940 recalls

FDA records 2 decisions for Matrix Electromedical, Inc. (Las Vegas, NV) from 1993 to 1994: 2 510(k) clearances. All are in product code LIH (Interferential Current Therapy). 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 Matrix Electromedical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Matrix Electromedical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Matrix Electromedical, 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 “Matrix”

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

Matrix Medica, Inc. 14 Matrix Instruments 4 Matrix Technologies Corp. 3 Matrix Surgical Holdings, LLC/Matrix Surgical USA 2 Matrix Biokinetics, Inc. 1 Matrix Surgical USA 1 Matrix Intl. 1

Matrix Electromedical, 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 “Matrix”