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Prometal Technologies

Country not established

Devices
1

What Prometal Technologies makes

Prometal Technologies manufactures the PROMETAL HN86, a medical device designed for orthopedic applications, specifically for use in spinal fixation procedures.

The PROMETAL HN86 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

  • Prometal HN86 Ref K052463

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

Frequently asked questions

How many devices does Prometal Technologies have in the registry?

The registry currently lists 1 device for Prometal Technologies. Devices recorded under merged duplicate company entries are counted once.

Which registries list Prometal Technologies's devices?

Among its 1 most recently registered device, Prometal Technologies has devices listed in FDA 510(k) (1 device).

What risk classes do Prometal Technologies's devices fall under?

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

What are the newest devices from Prometal Technologies in the registry?

The most recently registered devices listed for Prometal Technologies include PROMETAL HN86.

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