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Richway Intl., Inc.

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Devices
1

What Richway Intl., Inc. makes

Richway Intl., Inc. manufactures the BIO-MAT 2000, a medical device designed for tissue integration or wound management applications.

The BIO-MAT 2000 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. 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

  • Bio-Mat 2000 Ref K072534

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

Frequently asked questions

How many devices does Richway Intl., Inc. have in the registry?

The registry currently lists 1 device for Richway Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Richway Intl., Inc.'s devices?

Among its 1 most recently registered device, Richway Intl., Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Richway Intl., Inc.'s devices fall under?

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

What are the newest devices from Richway Intl., Inc. in the registry?

The most recently registered devices listed for Richway Intl., Inc. include BIO-MAT 2000.

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