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Noromed, Inc.

United StatesFDA applicant, unverified

Devices
2

What Noromed, Inc. makes

Noromed, Inc. manufactures the NORODYN 2000 Electromyograph, a device used for assessing muscle electrical activity, and the NOROTRACK 360 Inclinometer, which measures angles of body positioning or movement for clinical or research applications.

The company’s products are regulated under FDA Class I and Class II classifications, with the NORODYN 2000 and NOROTRACK 360 listed in the FDA’s 510(k) registry. Noromed, Inc. 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

  • Norodyn 2000 Electromyograph Ref K922838

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Norotrack 360 Inclinometer Ref K920690

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

Frequently asked questions

How many devices does Noromed, Inc. have in the registry?

The registry currently lists 2 devices for Noromed, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Noromed, Inc.'s devices?

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

What risk classes do Noromed, Inc.'s devices fall under?

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

What are the newest devices from Noromed, Inc. in the registry?

The most recently registered devices listed for Noromed, Inc. include NORODYN 2000 ELECTROMYOGRAPH and NOROTRACK 360 INCLINOMETER.

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