FDA applicant

Mwi, Inc.

Dallas, TX1 decision1999–19994 recalls

FDA records 1 decision for Mwi, Inc. (Dallas, TX) in 1999: 1 510(k) clearance. All are in product code GKZ (Counter, Differential Cell). Its devices cite 2 predicates, 0 of them its own earlier devices. 4 recalls are 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 Mwi, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mwi, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mwi, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?