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G-Ortho Lab

Country not established

Devices
1

What G-Ortho Lab makes

G-Ortho Lab manufactures the NAPA, a medical device designed for orthopedic applications, likely used in the treatment or assessment of lower limb alignment or joint positioning.

The company’s portfolio is regulated under FDA Class II devices, with the NAPA authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry, and the manufacturer 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

  • Napa Ref K902790

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does G-Ortho Lab have in the registry?

The registry currently lists 1 device for G-Ortho Lab. Devices recorded under merged duplicate company entries are counted once.

Which registries list G-Ortho Lab's devices?

Among its 1 most recently registered device, G-Ortho Lab has devices listed in FDA 510(k) (1 device).

What risk classes do G-Ortho Lab's devices fall under?

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

What are the newest devices from G-Ortho Lab in the registry?

The most recently registered devices listed for G-Ortho Lab include NAPA.

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