Skip to content

Unicare Medical Products, Inc.

CanadaFDA applicant, unverified

Devices
1

What Unicare Medical Products, Inc. makes

Unicare Medical Products, Inc. manufactures breast shells, which are reusable devices used to support and protect the breast during and after breast surgery or radiation therapy.

The company’s breast shells are classified as Class I medical devices in the US and are listed under the FDA’s 510(k) pathway. The portfolio is regulated under US jurisdiction.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Unicare Breast Shells Ref K861608

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

Frequently asked questions

How many devices does Unicare Medical Products, Inc. have in the registry?

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

Which registries list Unicare Medical Products, Inc.'s devices?

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

What risk classes do Unicare Medical Products, Inc.'s devices fall under?

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

What are the newest devices from Unicare Medical Products, Inc. in the registry?

The most recently registered devices listed for Unicare Medical Products, Inc. include UNICARE BREAST SHELLS.

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