FDA applicant

Medical Diagnostic Technologies, Inc.

Ventura, CA57 decisions1985–20060 recalls

FDA records 57 decisions for Medical Diagnostic Technologies, Inc. (Ventura, CA) from 1985 to 2006: 57 510(k) clearances. Most are in product codes GJT (Plasma, Coagulation Factor Deficient) and GGP (Test, Qualitative And Quantitative Factor…). Its devices cite 4 predicates, 0 of them its own earlier devices. 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 Medical Diagnostic Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Diagnostic Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Medical Diagnostic Technologies, 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?