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North American Philips Corp.

United StatesFDA applicant, unverified

Devices
15

What North American Philips Corp. makes

The company manufactures blood pressure measurement devices, including aneroid cuffs, analog electronic meters, and digital blood pressure monitors. It also produces electronic digital thermometers for fever measurement and vibrating massage belts with heat functions.

These devices are regulated under the FDA’s 510(k) pathway, with most classified as Class I or Class II medical devices. The portfolio is listed in the FDA’s 510(k) clearance registry, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does North American Philips Corp. have in the registry?

The registry currently lists 15 devices for North American Philips Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list North American Philips Corp.'s devices?

Among its 15 most recently registered devices, North American Philips Corp. has devices listed in FDA 510(k) (15 devices).

What risk classes do North American Philips Corp.'s devices fall under?

Among its 15 most recently registered devices, the classes recorded for North American Philips Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from North American Philips Corp. in the registry?

The most recently registered devices listed for North American Philips Corp. include NORELCO ANEROID BLOOD PRESSURE METER, NORELCO MASSAGER PLUS HEAT BELT, NORELCO DELUXE DIGITAL BLOOD PRESSURE and NORELCO ELECTRONIC BLOOD PRESSURE METER.

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