FDA applicant

Diapharma Group, Inc.

West Chester, OH1 decision2004–20040 recalls

FDA records 1 decision for Diapharma Group, Inc. (West Chester, OH) in 2004: 1 510(k) clearance. All are in product code GJT (Plasma, Coagulation Factor Deficient). 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 Diapharma Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diapharma Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Diapharma Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?