FDA applicant

Raymax Medical Corp.

Ontario, L4l 7k5, CA3 decisions1988–19930 recalls

FDA records 3 decisions for Raymax Medical Corp. (Ontario, L4l 7k5, CA) from 1988 to 1993: 3 510(k) clearances. Most are in product codes JAA (System, X-Ray, Fluoroscopic, Image-Intensified) and IZZ (Table, Radiographic, Non-Tilting, Powered). 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 Raymax Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Raymax Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Raymax Medical Corp.

Which product codes does it file in?

What has FDA decided for it lately?