FDA applicant

M. D. Products

Ocala, FL3 decisions1987–19900 recalls

FDA records 3 decisions for M. D. Products (Ocala, FL) from 1987 to 1990: 3 510(k) clearances. Most are in product codes LWM (Device, Electrical Dental Anesthesia) and ITY (Assembly, Tube Housing, X-Ray, Diagnostic). 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, radiology panel, where it files most

How often FDA has decided M. D. Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for M. D. Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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M. D. Products

Which product codes does it file in?

What has FDA decided for it lately?