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Oxti Corporation

Country not established

Devices
1

What Oxti Corporation makes

Oxti Corporation manufactures an inflation device designed for medical applications, likely used in procedures requiring controlled pressure or volume delivery.

The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) premarket notification database. 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

  • Oxti Inflation Device Ref K122152

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

Frequently asked questions

How many devices does Oxti Corporation have in the registry?

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

Which registries list Oxti Corporation's devices?

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

What risk classes do Oxti Corporation's devices fall under?

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

What are the newest devices from Oxti Corporation in the registry?

The most recently registered devices listed for Oxti Corporation include OXTI INFLATION DEVICE.

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