FDA applicant

Omron Marshall Products, Inc.

Lincolnshire, IL3 decisions1990–19910 recalls

FDA records 3 decisions for Omron Marshall Products, Inc. (Lincolnshire, IL) from 1990 to 1991: 3 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and JEQ (Toothbrush, Powered). 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, cardiovascular panel, where it files most

How often FDA has decided Omron Marshall Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Omron Marshall Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Omron Marshall Products, 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 “Omron”

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

Omron Healthcare, Inc. 69 Omron Electronics, Inc. 10 Omron Tateisi Electronics Co. 7

Omron Marshall Products, 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 “Omron”