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Iyia Technologies, Inc.

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Devices
1

What Iyia Technologies, Inc. makes

Iyia Technologies, Inc. manufactures the WHS-1000 Wound Healing System, a device designed for the treatment and management of chronic or acute wounds in clinical settings.

The WHS-1000 is classified as a Class II medical 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

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Frequently asked questions

How many devices does Iyia Technologies, Inc. have in the registry?

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

Which registries list Iyia Technologies, Inc.'s devices?

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

What risk classes do Iyia Technologies, Inc.'s devices fall under?

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

What are the newest devices from Iyia Technologies, Inc. in the registry?

The most recently registered devices listed for Iyia Technologies, Inc. include WHS-1000 WOUND HEALING SYSTEM.

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