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Hinatawada Seimitsu Mfg. Co., Ltd.

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Devices
1

What Hinatawada Seimitsu Mfg. Co., Ltd. makes

Hinatawada Seimitsu Mfg. Co., Ltd. manufactures the AIR MEDICA III, a medical device designed for respiratory support or oxygen delivery.

The device is classified as Class I under FDA regulations and is listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Air Medica Iii Ref K920710

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

Frequently asked questions

How many devices does Hinatawada Seimitsu Mfg. Co., Ltd. have in the registry?

The registry currently lists 1 device for Hinatawada Seimitsu Mfg. Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hinatawada Seimitsu Mfg. Co., Ltd.'s devices?

Among its 1 most recently registered device, Hinatawada Seimitsu Mfg. Co., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Hinatawada Seimitsu Mfg. Co., Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Hinatawada Seimitsu Mfg. Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Hinatawada Seimitsu Mfg. Co., Ltd. in the registry?

The most recently registered devices listed for Hinatawada Seimitsu Mfg. Co., Ltd. include AIR MEDICA III.

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