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Mednova Corp.

United StatesFDA applicant, unverified

Devices
2

What Mednova Corp. makes

Mednova Corp. manufactures a blood pressure cuff for non-invasive monitoring of arterial pressure and a safety bag designed for the containment and disposal of sharps or contaminated medical waste.

The company’s products are classified as Class II devices under FDA regulations and are listed in the 510(k) clearance registry. Mednova Corp. is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Mednova Blood Pressure Cuff Ref K854813

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Mednova Safety Bag Ref K853075

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

Frequently asked questions

How many devices does Mednova Corp. have in the registry?

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

Which registries list Mednova Corp.'s devices?

Among its 2 most recently registered devices, Mednova Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Mednova Corp.'s devices fall under?

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

What are the newest devices from Mednova Corp. in the registry?

The most recently registered devices listed for Mednova Corp. include MEDNOVA BLOOD PRESSURE CUFF and MEDNOVA SAFETY BAG.

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