FDA applicant

Medicus Technologies, Inc.

West Chester, PA1 decision1996–19960 recalls

FDA records 1 decision for Medicus Technologies, Inc. (West Chester, PA) in 1996: 1 510(k) clearance. All are in product code GIQ (Hemoglobin S). 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, hematology panel, where it files most

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

FDA decisions per year

No FDA decision for Medicus Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medicus Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?