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Lorin Medical, Inc.

Country not established

Devices
1

What Lorin Medical, Inc. makes

Lorin Medical, Inc. manufactures the CUFF-M, a medical device designed for blood pressure monitoring and cuff-based measurements in clinical settings.

The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. Lorin Medical, Inc. is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Cuff-M Ref K921997

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

Frequently asked questions

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

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

Which registries list Lorin Medical, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Lorin Medical, Inc. include CUFF-M.

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