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Sign in to claim this brandBio-Medical Science & Technology LIMITED
US
Last updated May 25, 2026
What Bio-Medical Science & Technology LIMITED makes
Bio-Medical Science & Technology LIMITED produces single-use transcutaneous electrical stimulation electrodes, such as the Slendertone Replacement Abdominal Toning Gel Pads, and physical therapy systems like the Slendertone for neuromuscular electrical stimulation.
Their devices are classified as Class II and listed in the FDA’s Unique Device Identifier (UDI) database, with the company headquartered 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 Bio-Medical Science & Technology LIMITED manufacture?
Bio-Medical Science & Technology LIMITED specializes in two primary categories of devices: single-use transcutaneous electrical stimulation electrodes (such as the Slendertone Replacement Abdominal Toning Gel Pads) and physical therapy systems for transcutaneous neuromuscular electrical stimulation (like the Slendertone). These devices are designed to deliver targeted electrical stimulation for therapeutic or wellness purposes.
Where is Bio-Medical Science & Technology LIMITED based?
The company is headquartered in the United States. This location is relevant for regulatory and compliance purposes, as it influences the jurisdiction under which its devices may be authorized.
Which regulatory registries or databases list Bio-Medical Science & Technology LIMITED’s devices?
The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices for regulatory, traceability, and compliance purposes, ensuring transparency in the supply chain.
How are Bio-Medical Science & Technology LIMITED’s devices classified under medical device regulations?
The devices produced by Bio-Medical Science & Technology LIMITED fall under Class II classification. This classification is determined based on factors like risk level, intended use, and potential health impact, requiring specific regulatory controls to ensure safety and effectiveness.
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
- 986121542
Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Slendertone Replacement Abdominal Toning Gel Pads | Type 732 & 733 | FDA UDI | Class II | Active |
| Slendertone | Type 735 | FDA UDI | Class II | Active |
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