Skip to content

Capcard, Inc.

Country not established

Devices
1

What Capcard, Inc. makes

Capcard, Inc. manufactures the CAPCARD, a medical device designed for patient identification and wristband management in healthcare settings. It integrates with electronic health record systems to reduce errors in patient identification and improve workflow efficiency.

The CAPCARD is classified as a Class II device under FDA regulations and has been authorised through the 510(k) clearance process. 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

  • Capcard Ref K942930

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

Frequently asked questions

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

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

Which registries list Capcard, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Capcard, Inc. include CAPCARD.

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