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Merex Co.

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Devices
1

What Merex Co. makes

Merex Co. manufactures HOSPITAL'S-SPEC, a customizable hospital-grade device designed for specialized medical environments. These products are tailored to meet specific institutional requirements, ensuring compatibility with existing workflows and infrastructure.

The company’s portfolio is regulated under FDA Class II devices, with products listed via 510(k) clearance. The manufacturer operates from the United States, adhering to U.S. regulatory standards for medical devices.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Hospital's-Spec Ref K842014

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

Frequently asked questions

How many devices does Merex Co. have in the registry?

The registry currently lists 1 device for Merex Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Merex Co.'s devices?

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

What risk classes do Merex Co.'s devices fall under?

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

What are the newest devices from Merex Co. in the registry?

The most recently registered devices listed for Merex Co. include HOSPITAL'S-SPEC.

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