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FORANS SIA

US

Last updated May 27, 2026

What FORANS SIA makes

Forans SIA manufactures portable electronic devices for measuring blood pressure and body temperature. Their products include automatic-inflation sphygmomanometers designed for arm or wrist use, as well as infrared thermometers for non-contact ear or forehead readings. These devices are intended for clinical and home monitoring applications.

The company’s devices are classified as Class II under regulatory frameworks and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are developed and distributed from their base in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Forans SIA manufacture?

Forans SIA produces portable electronic devices focused on monitoring vital signs. Their primary offerings include automatic-inflation electronic sphygmomanometers for measuring blood pressure on the arm or wrist, as well as infrared thermometers designed for non-contact temperature readings in the ear or on the forehead. These devices are intended for use in both clinical settings and home monitoring.

Where is Forans SIA based, and where are their devices manufactured or distributed?

Forans SIA is based in the United States. While the provided data does not specify manufacturing locations, their devices are developed and distributed from their US headquarters, targeting global markets for clinical and home use.

Which regulatory registries list Forans SIA’s devices?

Forans SIA’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorised for commercial distribution in the United States, ensuring traceability and compliance with regulatory requirements.

How are Forans SIA’s devices classified under regulatory frameworks?

Forans SIA’s devices fall under Class II classification in regulatory frameworks. This classification typically applies to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as blood pressure monitors and infrared thermometers, which require validation of performance and labeling standards.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
365515625

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
EVOLU Non Contact Infrared Ear/Forehead Thermometer PG-IRT1603
FDA UDI
Class IIActive
EVOLU Intelligent Blood Pressure Monitor PG-800B19L
FDA UDI
Class IIActive

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