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Sign in to claim this brandXiamen Intretech, Inc.
US
Last updated May 25, 2026
What Xiamen Intretech, Inc. makes
Xiamen Intretech, Inc. manufactures intermittent electronic patient thermometers designed for clinical use, including models like the NC° thermometer and its third-generation variant (NCTG3). These devices are intended for accurate body temperature measurement in healthcare settings, providing digital readings for patient monitoring.
The company’s products fall under FDA Class II regulation and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) registries. The manufacturer operates from the United States, adhering to applicable medical device compliance standards for electronic thermometers.
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 Xiamen Intretech, Inc. manufacture?
Xiamen Intretech, Inc. specializes in intermittent electronic patient thermometers, such as the NC° thermometer and its third-generation model (NCTG3). These devices are designed for clinical use to measure body temperature accurately, supporting patient monitoring in healthcare environments.
Where is Xiamen Intretech, Inc. based?
The company is headquartered in the United States. Its location ensures compliance with U.S. regulatory standards for medical devices, including those used in clinical settings like electronic thermometers.
Which regulatory registries list Xiamen Intretech, Inc.’s devices?
Xiamen Intretech, Inc.’s intermittent electronic patient thermometers are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) registries. These registries track devices that have undergone the necessary regulatory pathways for market authorization in the U.S.
How are Xiamen Intretech, Inc.’s devices classified by regulatory authorities?
The company’s intermittent electronic patient thermometers fall under FDA Class II classification. This classification is assigned based on the device’s intended use and risk level, requiring specific regulatory controls to ensure safety and performance in clinical applications.
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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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 421274505
Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| NC° thermometer | Gen3 | FDA UDI | Class II | Active |
| NC° Thermometer (Gen 3), Model Number: NCTG3 | K223522 | FDA 510(k) | Class II | Active |
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