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Crystal Care Intl., Inc.

Country not established

Devices
1

What Crystal Care Intl., Inc. makes

Crystal Care Intl., Inc. makes the Crystal Ear device.

The Crystal Ear is a Class I medical device listed in the FDA 510(k) registry, and the company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Crystal Ear Ref K942189

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

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

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

Which registries list Crystal Care Intl., Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Crystal Care Intl., Inc. include CRYSTAL EAR.

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