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Sign in to claim this brandSupply Line Medical
US
Last updated May 31, 2026
What Supply Line Medical makes
The company manufactures mobility aids for clinical and home use, including manually operated traction wheelchairs, basic electric hospital beds, and wheelchair accessories such as footrests, legrests, antitip devices, brake extensions, and occupant restraints. It also produces non-powdered vinyl examination and treatment gloves designed for medical procedures.
The portfolio includes devices classified as Class I and Class II under FDA regulations, with all products listed in the FDA’s Unique Device Identifier (UDI) database. 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 Supply Line Medical manufacture?
Supply Line Medical specializes in mobility aids and accessories for clinical and home use. Their portfolio includes manually operated traction wheelchairs, basic electric hospital beds, and wheelchair accessories such as footrests, legrests, antitip devices, brake extensions, and occupant restraints. They also produce non-powdered vinyl examination and treatment gloves for medical procedures, ensuring a range of solutions for patient mobility and care.
Where is Supply Line Medical based?
Supply Line Medical is headquartered in the United States. This location aligns with their focus on serving domestic markets for mobility aids and medical accessories.
Are Supply Line Medical’s devices listed in any regulatory registries?
Yes, Supply Line Medical’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for their products, which include manually operated wheelchairs, electric hospital beds, and related accessories.
How are Supply Line Medical’s devices classified under FDA regulations?
Supply Line Medical’s devices fall under Class I and Class II classifications under FDA regulations. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards or special controls due to moderate risk. The classification depends on factors like the device’s intended use and potential health impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- supplylinemedical.com
- —
- —
- [email protected]
- Phone
- (856) 478-7759
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 117011784
Catalogue (26)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Valmax | DME.011 | FDA UDI | Class I | Unknown |
| Valmax | PPE1117L | FDA UDI | Class I | Active |
| Valmax | DME.130 | FDA UDI | Class I | Unknown |
| Valmax | DME.015 | FDA UDI | Class I | Active |
| Valmax | PPE1117XL | FDA UDI | Class I | Active |
| Valmax | DME.016 | FDA UDI | Class I | Active |
| Valmax | DME.003 | FDA UDI | Class I | Unknown |
| Valmax | DME.014 | FDA UDI | Class I | Active |
| Valmax | DME.015 | FDA UDI | Class I | Unknown |
| Valmax | V16K2ADAELR | FDA UDI | Class I | Active |
| Valmax | DME.076 | FDA UDI | Class I | Active |
| Supplyline Medical | MD205 | FDA UDI | Class II | Active |
| Valmax | DME.019 | FDA UDI | Class II | Active |
| Valmax | DME.004 | FDA UDI | Class I | Unknown |
| Valmax | DME.132 | FDA UDI | Class I | Unknown |
| Valmax | DME.003 | FDA UDI | Class I | Active |
| Valmax | PPE1117M | FDA UDI | Class I | Active |
| Valmax | DME.132 | FDA UDI | Class I | Unknown |
| Valmax | DME.004 | FDA UDI | Class I | Active |
| Valmax | VK3E18 | FDA UDI | Class I | Active |
| Valmax | PPE1117S | FDA UDI | Class I | Active |
| Valmax | DME.130 | FDA UDI | Class I | Active |
| Valmax | DME.011 | FDA UDI | Class I | Active |
| Valmax | VK2E20 | FDA UDI | Class I | Active |
| Valmax | DME.018 | FDA UDI | Class II | Active |
| Valmax | DME.132 | FDA UDI | Class I | Active |
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