FDA applicant

Matrix Instruments

Orangeburg, NY4 decisions1984–19870 recalls

FDA records 4 decisions for Matrix Instruments (Orangeburg, NY) from 1984 to 1987: 4 510(k) clearances. Most are in product codes IZI (System, X-Ray, Angiographic) and LMC (Camera, Multi Format, Radiological). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Matrix Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Matrix Instruments 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 Technologies Corp. 3 Matrix Electromedical, Inc. 2 Matrix Surgical Holdings, LLC/Matrix Surgical USA 2 Matrix Biokinetics, Inc. 1 Matrix Surgical USA 1 Matrix Intl. 1

Matrix Instruments

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Matrix”