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Sign in to claim this brandInfervision Medical Technology Co., Ltd
US
Last updated May 30, 2026
What Infervision Medical Technology Co., Ltd makes
Infervision Medical Technology Co., Ltd makes diagnostic x-ray digital imaging system workstations and x-ray image interpretive software. One example of their product is InferRead Lung CT.AI, which is used for analyzing lung CT scans.
The company's devices are classified as Class II medical devices and are listed in the FDA's Unique Device Identification (FDA UDI) system. Infervision Medical Technology Co., Ltd is based 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 does Infervision Medical Technology Co., Ltd make?
Infervision Medical Technology Co., Ltd makes diagnostic x-ray digital imaging system workstations and x-ray image interpretive software, as stated in the device data. One example of their product is InferRead Lung CT.AI, which is used for analyzing lung CT scans. This indicates their focus on software and workstation solutions for medical imaging analysis.
Where is Infervision Medical Technology Co., Ltd based?
Infervision Medical Technology Co., Ltd is based in the United States, as explicitly stated in the device data under the COUNTRY field and reiterated in the SUMMARY. This location refers to the company's headquarters or primary operational base as provided in the source information.
Which regulatory registries list devices from Infervision Medical Technology Co., Ltd?
Devices from Infervision Medical Technology Co., Ltd are listed in the FDA's Unique Device Identification (FDA UDI) system, as indicated in the LISTED IN field of the device data. This means their devices have been assigned UDIs and are included in the FDA’s public database for device tracking and identification.
How are the devices made by Infervision Medical Technology Co., Ltd classified?
The devices made by Infervision Medical Technology Co., Ltd are classified as Class II medical devices, as specified in the DEVICE CLASSES field of the device data. This classification reflects the level of regulatory control required to ensure safety and effectiveness, based on the device’s intended use and risk profile.
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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- 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
- 551093752
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| InferRead Lung CT.AI | 5.0.2.5 | FDA UDI | Class II | Active |
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