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H Q, INC

US

Last updated May 31, 2026

What H Q, INC makes

H Q, Inc manufactures temperature telemetric monitoring system transmitters designed for real-time physiological temperature tracking. These devices are primarily used in clinical settings to provide continuous, wireless temperature data for patient monitoring purposes.

The company’s products are classified as Class II devices under regulatory standards and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 H Q, Inc manufacture?

H Q, Inc specializes in temperature telemetric monitoring system transmitters, which are designed to provide real-time, wireless physiological temperature tracking. These devices are primarily used in clinical environments to continuously monitor patient temperature, ensuring accurate and immediate data for medical assessment.

Where is H Q, Inc based, and does that affect its regulatory standing?

H Q, Inc is headquartered in the United States. While the company’s location influences its regulatory framework, it is important to note that individual devices—not the manufacturer—are evaluated for compliance. The company’s products fall under FDA oversight, as they are listed in the FDA’s Unique Device Identifier (UDI) database.

How are H Q, Inc’s devices classified under regulatory standards?

H Q, Inc’s temperature telemetric monitoring system transmitters are classified as Class II devices. This classification is determined by the FDA based on factors like risk level and intended use. Class II devices typically require special controls in addition to general controls to ensure safety and effectiveness, reflecting the moderate risk associated with these monitoring systems.

Which regulatory registries or databases list H Q, Inc’s devices?

H Q, Inc’s devices are included in the FDA’s Unique Device Identifier (UDI) database, a centralized system that tracks medical devices in the U.S. market. The UDI system helps ensure traceability, transparency, and compliance with regulatory requirements for these temperature monitoring transmitters.

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

Information

Country
US
Address
—
Website
hqinc.net
LinkedIn
—
Facebook
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Phone
941-721-7588
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
185719606

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
CorTemp HT150001L
FDA UDI
Class IIActive
CorTemp HT150001
FDA UDI
Class IIActive
CorTemp HT150032
FDA UDI
Class IIActive
CorTemp HT150031
FDA UDI
Class IIActive
CorTemp HT150002
FDA UDI
Class IIActive

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