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The Medipattern Corporation

CanadaFDA applicant, unverified

Devices
2

What The Medipattern Corporation makes

The Medipattern Corporation makes the B-CAD System, Version 1.0, and the Visualize: Vascular device.

These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • B-Cad System, Version 1.0 Ref K050846

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Visualize: Vascular Ref K103761

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does The Medipattern Corporation have in the registry?

The registry currently lists 2 devices for The Medipattern Corporation. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Medipattern Corporation's devices?

Among its 2 most recently registered devices, The Medipattern Corporation has devices listed in FDA 510(k) (2 devices).

What risk classes do The Medipattern Corporation's devices fall under?

Among its 2 most recently registered devices, the classes recorded for The Medipattern Corporation's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from The Medipattern Corporation in the registry?

The most recently registered devices listed for The Medipattern Corporation include B-CAD SYSTEM, VERSION 1.0 and VISUALIZE: VASCULAR.

Generated automatically from registry data and not verified by a human reviewer.