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Sign in to claim this brandRaling Medical Company
US
Last updated May 23, 2026
What Raling Medical Company makes
Raling Medical Company manufactures wireless thermometers designed for clinical and patient monitoring applications. These devices are intended to provide accurate temperature readings remotely, supporting real-time patient assessment in healthcare settings.
The company’s wireless thermometers are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. These products are intended for use within 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 Raling Medical Company manufacture?
Raling Medical Company specializes in wireless thermometers. These devices are engineered for clinical and patient monitoring, enabling accurate temperature readings to be transmitted wirelessly. This design supports real-time patient assessment in healthcare environments, particularly where remote or continuous monitoring is beneficial.
Where is Raling Medical Company based?
Raling Medical Company is headquartered in the United States. The company’s focus on wireless thermometers aligns with regulatory frameworks applicable in the US market, including those governed by the FDA.
How are Raling Medical Company’s devices classified under FDA regulations?
Raling Medical Company’s wireless thermometers fall under Class II classification according to FDA guidelines. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance. The Class II designation reflects the need for regulatory oversight while balancing innovation in remote monitoring solutions.
Which regulatory registries or pathways list Raling Medical Company’s devices?
Raling Medical Company’s wireless thermometers are listed via the FDA’s 510(k) pathway. This pathway demonstrates that the devices are substantially equivalent to a legally marketed predicate device, meeting FDA requirements for safety and performance. Listing in this registry confirms compliance with US regulatory standards for Class II devices.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| raiing iThermonitor | WT701 | FDA UDI | Class II | Active |
| raiing iFertracker | WT702 | FDA UDI | U | Active |
| Fridababy | WT701 | FDA UDI | Class II | Active |
| raiing iThermonitor | WT701 | FDA UDI | Class II | Active |
| Caring Mill | WT701 | FDA UDI | Class II | Active |
| Wireless Thermometer | K132761 | FDA 510(k) | Class II | Active |
| Wireless Thermometer | K121696 | FDA 510(k) | Class II | Active |
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