FDA applicant

Midi, Inc.

Newark, DE2 decisions2002–20060 recalls

FDA records 2 decisions for Midi, Inc. (Newark, DE) from 2002 to 2006: 2 510(k) clearances. Most are in product codes NJO (System, Mycolic Acid Analysis, Mycobacterium…) and NWZ (Gas Chromatography, Bacillus Anthracis…). 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, microbiology panel, where it files most

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

FDA decisions per year

No FDA decision for Midi, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Midi, Inc.

Which product codes does it file in?

What has FDA decided for it lately?