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Sign in to claim this brandAd Rem Technology Sarl
US
Last updated May 23, 2026
What Ad Rem Technology Sarl makes
Ad Rem Technology Sarl manufactures neuromuscular stimulators, including the Veinoplus Sport and Veinoplus models, designed for medical use in venous health applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. 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 Ad Rem Technology Sarl manufacture?
Ad Rem Technology Sarl specializes in neuromuscular stimulators, specifically the Veinoplus Sport and Veinoplus models. These devices are intended for medical use in venous health applications, helping to improve circulation and reduce symptoms like swelling or discomfort.
Where is Ad Rem Technology Sarl based?
Ad Rem Technology Sarl is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution, as it operates within the FDA’s jurisdiction.
How are Ad Rem Technology Sarl’s devices classified under FDA regulations?
Ad Rem Technology Sarl’s neuromuscular stimulators, including the Veinoplus Sport and Veinoplus models, are classified as Class II devices by the FDA. This classification is based on their intended use in venous health, where they pose moderate risk and require special controls to ensure safety and effectiveness.
Which regulatory registries or pathways list Ad Rem Technology Sarl’s devices?
Ad Rem Technology Sarl’s neuromuscular stimulators are listed via the FDA’s 510(k) pathway, meaning their devices have been determined to be substantially equivalent to a legally marketed predicate device. This pathway is used for Class II devices where the manufacturer demonstrates that their product is as safe and effective as an existing, cleared device.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (6)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Veinoplus Pack | 8x13 OVAL | FDA UDI | Class II | Active |
| Veinoplus | 2.1 | FDA UDI | Class II | Active |
| Veinoplus Sport | 2.1 | FDA UDI | Class II | Active |
| Veinoplus Dvt | 2.1 | FDA UDI | Class II | Active |
| Veinoplus Sport Neuromuscular Stimulator | K141919 | FDA 510(k) | Class II | Active |
| Veinoplus Neuromuscular Stimulator | K072252 | FDA 510(k) | Class II | Active |
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