FDA applicant

Matrix Technologies Corp.

Lowell, MA3 decisions1991–19960 recalls

FDA records 3 decisions for Matrix Technologies Corp. (Lowell, MA) from 1991 to 1996: 3 510(k) clearances. All are in product code JQW (Station, Pipetting And Diluting, For Clinical…). 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, clinical chemistry panel, where it files most

How often FDA has decided Matrix Technologies Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Matrix Technologies Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Matrix Technologies Corp. 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 Electromedical, Inc. 2 Matrix Surgical Holdings, LLC/Matrix Surgical USA 2 Matrix Biokinetics, Inc. 1 Matrix Surgical USA 1 Matrix Intl. 1

Matrix Technologies Corp.

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”