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Sign in to claim this brandCAF MEDICAL SOLUTIONS INC
US
Last updated September 17, 2026
What CAF MEDICAL SOLUTIONS INC makes
Caf Medical Solutions Inc manufactures general-purpose multi-parameter bedside monitors and professional multichannel electrocardiographs. The example devices listed are all variations of the LIFEE product line.
These devices are classified as Class II medical devices and are listed in the FDA UDI registry. The company 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 types of medical devices does CAF Medical Solutions Inc manufacture?
CAF Medical Solutions Inc produces two main categories of devices: general‑purpose multi‑parameter bedside monitors and professional multichannel electrocardiographs. This is derived directly from the listed device categories, indicating the company focuses on patient monitoring and cardiac diagnostics.
Where is CAF Medical Solutions Inc located and where are its devices registered?
The company is based in the United States, as stated in the country field. Its devices are listed in the FDA UDI registry, which is the official United States database for unique device identification, confirming the regulatory listing location.
How are the devices from CAF Medical Solutions Inc classified under U.S. regulations?
All devices from CAF Medical Solutions Inc are classified as Class II medical devices. This classification is explicitly provided in the device classes section and reflects the regulatory risk level assigned to their bedside monitors and electrocardiographs.
What is the product line name for the devices offered by CAF Medical Solutions Inc?
The example devices are all variations of the LIFEE product line. The repeated listing of LIFEE under example devices indicates that this is the brand or model name used for both the bedside monitors and electrocardiographs.
Are CAF Medical Solutions Inc’s devices approved or cleared by any authority?
The information only states that the devices are listed in the FDA UDI registry and classified as Class II; it does not claim any approval, certification, or clearance. Therefore, while they are registered, the text does not assert that any specific device has received regulatory approval.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 17539 Roberts Road, Hockley, TX, 77447
- 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
- 3021559257
- DUNS Number
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Catalogue (11)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Lifee | LMPLUS-12 | FDA UDI | Class II | Active |
| Lifee | LM-8 | FDA UDI | Class II | Active |
| Lifee | LM-10 | FDA UDI | Class II | Active |
| Lifee | LMPLUS-15 | FDA UDI | Class II | Active |
| Lifee | LMPLUS-17 | FDA UDI | Class II | Active |
| Lifee | LM-15 | FDA UDI | Class II | Active |
| Lifee | LM-12 | FDA UDI | Class II | Active |
| Lifee | LE-12CH | FDA UDI | Class II | Active |
| Patient Monitor, models LM-8, LM-10, LM-12 and LM-15 | K221879 | FDA 510(k) | Class II | Active |
| Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17 | K221616 | FDA 510(k) | Class II | Active |
| Le-12ch | K220362 | FDA 510(k) | Class II | Active |
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