510(k) Report

FDA applicant

The Medipattern Corporation

Toronto, On, CA2 decisions2005–20110 recalls

FDA records 2 decisions for The Medipattern Corporation (Toronto, On, CA) from 2005 to 2011: 2 510(k) clearances. All are in product code LLZ (System, Image Processing, Radiological). Its devices cite 8 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, radiology panel, where it files most

How often FDA has decided The Medipattern Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011: 1
2007high 1 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Medipattern Corporation’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • LLZSystem, Image Processing, Radiological2decisions

Whose devices does it build on?

Its devices cite 8 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 5 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K050846B-Cad System, Version 1.0The Medipattern Corporation · 20055cite it

What has FDA decided for it lately?

  • K103761Visualize: VascularThe Medipattern Corporation · 2011
  • K050846B-Cad System, Version 1.0The Medipattern Corporation · 2005

All 2 as The Medipattern Corporation →