FDA applicant

Micromedical Industries, Ltd.

Northbrook, IL6 decisions1992–20021 recall

FDA records 6 decisions for Micromedical Industries, Ltd. (Northbrook, IL) from 1992 to 2002: 6 510(k) clearances. Most are in product codes LOS (Unnamed device) and MHX (Monitor, Physiological, Patient (With…). 1 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 Micromedical Industries, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micromedical Industries, Ltd. since 2007.

Recalls per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Micromedical”

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

Micromedical Devices, Inc. 7 Micromedical, Inc. 7 Micromedical Technologies, Inc. 5

Micromedical Industries, Ltd.

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?

What has been recalled?

Other applicant names beginning “Micromedical”