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New Horizon Health Care

Country not established

Devices
1

What New Horizon Health Care makes

New Horizon Health Care manufactures the NH-2002, a medical device designed for use in spinal surgery, specifically as an interbody fusion cage for lumbar and thoracic applications.

The NH-2002 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Nh-2002 Ref K932050

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

Frequently asked questions

How many devices does New Horizon Health Care have in the registry?

The registry currently lists 1 device for New Horizon Health Care. Devices recorded under merged duplicate company entries are counted once.

Which registries list New Horizon Health Care's devices?

Among its 1 most recently registered device, New Horizon Health Care has devices listed in FDA 510(k) (1 device).

What risk classes do New Horizon Health Care's devices fall under?

Among its 1 most recently registered device, the classes recorded for New Horizon Health Care's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from New Horizon Health Care in the registry?

The most recently registered devices listed for New Horizon Health Care include NH-2002.

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