FDA applicant

The Medical Device Group, Inc.

Crofton, MD1 decision2002–20021 recall

FDA records 1 decision for The Medical Device Group, Inc. (Crofton, MD) in 2002: 1 510(k) clearance. All are in product code MOD (Accessory To Continuous Ventilator (Respirator)). 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, anesthesiology panel, where it files most

How often FDA has decided The Medical Device Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Medical Device Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Medical Device Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?