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St. Croix Medical Systems, Inc.

Country not established

Devices
1

What St. Croix Medical Systems, Inc. makes

St. Croix Medical Systems, Inc. manufactures the LIFE MONITOR I, a device designed for continuous monitoring of physiological parameters in critical care settings.

The LIFE MONITOR I is classified as a Class II medical device and is listed under the FDA’s 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

  • Life Monitor I Ref K842334

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

Frequently asked questions

How many devices does St. Croix Medical Systems, Inc. have in the registry?

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

Which registries list St. Croix Medical Systems, Inc.'s devices?

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

What risk classes do St. Croix Medical Systems, Inc.'s devices fall under?

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

What are the newest devices from St. Croix Medical Systems, Inc. in the registry?

The most recently registered devices listed for St. Croix Medical Systems, Inc. include LIFE MONITOR I.

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