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Marketing Consultants of America

Country not established

Devices
2

What Marketing Consultants of America makes

Marketing Consultants of America manufactures the TANARAMA, a medical device designed for [specific clinical purpose not provided in data]. The product is intended for [use case or patient population not detailed in data].

The TANARAMA is classified as a Class II device under FDA regulations and requires 510(k) clearance for market authorisation. The company operates within the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Tanarama Ref K812603

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Tanarama Ref K812543

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

Frequently asked questions

How many devices does Marketing Consultants of America have in the registry?

The registry currently lists 2 devices for Marketing Consultants of America. Devices recorded under merged duplicate company entries are counted once.

Which registries list Marketing Consultants of America's devices?

Among its 2 most recently registered devices, Marketing Consultants of America has devices listed in FDA 510(k) (2 devices).

What risk classes do Marketing Consultants of America's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Marketing Consultants of America's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Marketing Consultants of America in the registry?

The most recently registered devices listed for Marketing Consultants of America include TANARAMA.

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