FDA applicant

Matrix Medica, Inc.

Orchard Park, NY14 decisions1985–19960 recalls

FDA records 14 decisions for Matrix Medica, Inc. (Orchard Park, NY) from 1985 to 1996: 14 510(k) clearances. Most are in product codes EIA (Unit, Operative Dental) and BTM (Ventilator, Emergency, Manual (Resuscitator)). Its devices cite 2 predicates, 0 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, anesthesiology panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Matrix Medica, 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 “Matrix”

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

Matrix Instruments 4 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 Medica, 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 “Matrix”