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Zmed, Inc.

Country not established

Devices
1

What Zmed, Inc. makes

Zmed, Inc. produces the ZMED VP4000, a Class II medical device listed in the FDA 510(k) database.

The company is based in the United States and its device is regulated under the FDA's 510(k) pathway.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Zmed VP4000 Ref K130929

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

Frequently asked questions

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

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

Which registries list Zmed, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Zmed, Inc. include ZMED VP4000.

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