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Sign in to claim this brandNEUROTRON MEDICAL, INC.
US
Last updated May 25, 2026
What NEUROTRON MEDICAL, INC. makes
Neurotron Medical, Inc. manufactures single-use transcutaneous electrical stimulation electrodes, conductive media for electrodes, and diagnostic systems for peripheral nerve stimulation. Their portfolio includes devices like the PDC Restorer, Brevio, and TheraKnit, which are designed for therapeutic and diagnostic applications in nerve stimulation therapy.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. All devices are subject to FDA compliance requirements for electrical stimulation and diagnostic nerve stimulation systems.
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 Neurotron Medical, Inc. manufacture?
Neurotron Medical, Inc. specializes in three primary categories of devices: single-use transcutaneous electrical stimulation electrodes, electrode conductive media, and diagnostic peripheral nerve electrical stimulation systems. These products are designed for therapeutic and diagnostic applications in nerve stimulation therapy, such as pain management or nerve function assessment. Examples include devices like the PDC Restorer and Brevio.
Where is Neurotron Medical, Inc. based?
Neurotron Medical, Inc. is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.
Which regulatory registries list Neurotron Medical, Inc.’s devices?
Neurotron Medical, Inc.’s devices are listed in the FDA’s 510(k) database and the Unique Device Identifier (UDI) system. These registries track Class II medical devices that require premarket notification (510(k)) clearance or UDI compliance, ensuring traceability and regulatory oversight for electrical stimulation and diagnostic nerve stimulation systems.
How are Neurotron Medical, Inc.’s devices classified under FDA regulations?
Neurotron Medical, Inc.’s devices are classified as Class II medical devices by the FDA. This classification applies to products that generally pose moderate risk and require special controls—such as performance standards or post-market surveillance—to ensure safety and effectiveness. Examples include transcutaneous electrical stimulation electrodes and diagnostic nerve stimulation systems, which fall under this category due to their therapeutic and diagnostic applications.
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
- 147018519
Catalogue (63)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| PDC Restorer | PLB066-0400 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-2030 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-3030C | FDA UDI | Class II | Active |
| Brevio | BRV-0250 | FDA UDI | Class II | Active |
| Medical Science Products | PLB042-2030 | FDA UDI | Class II | Active |
| Precision DME | PLB030-3050D | FDA UDI | Class II | Active |
| TheraKnit | TKP-2030 | FDA UDI | Class II | Active |
| ReBuilder Medical | PLB033-0824 | FDA UDI | Class II | Active |
| Precision DME | PLB030-4115 | FDA UDI | Class II | Active |
| ReBuilder Medical | PLB033-0820 | FDA UDI | Class II | Active |
| Pinnacle West Medical | PLB071-3050 | FDA UDI | Class II | Active |
| ReBuilder Medical | PLB033-3015 | FDA UDI | Class II | Active |
| TheraKnit | TKG-3015 | FDA UDI | Class II | Active |
| ReBuilder Medical | PLB033-3017 | FDA UDI | Class II | Active |
| MediQuip | PLB068-3015 | FDA UDI | Class II | Active |
| Medical Science Products | PLB042-3050 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-3024C | FDA UDI | Class II | Active |
| ReBuilder Medical | PLB033-0822 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-3016C | FDA UDI | Class II | Active |
| TheraMist | TKA-0216 | FDA UDI | Class II | Active |
| TheraKnit | TKP-1080 | FDA UDI | Class II | Active |
| Tuttle Rehab | PLB051-2020C | FDA UDI | Class II | Active |
| ReBuilder Medical | PLB033-0826 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-0413 | FDA UDI | Class II | Active |
| TheraKnit | TKG-3020 | FDA UDI | Class II | Active |
| TheraKnit | TKK-001 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-3021C | FDA UDI | Class II | Active |
| TheraKnit | TKG-3022 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-3015C | FDA UDI | Class II | Active |
| Pinnacle West Medical | PLB071-1080 | FDA UDI | Class II | Active |
| Medical Science Products | PLB042-3019 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-3026C | FDA UDI | Class II | Active |
| Relief Medical | PLB043-3015 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-0216 | FDA UDI | Class II | Active |
| Relief Medical | PLB043-3016 | FDA UDI | Class II | Active |
| Pinnacle West Medical | PLB071-2030 | FDA UDI | Class II | Active |
| TheraKnit | TKG-3019 | FDA UDI | Class II | Active |
| Relief Combo | PLB043-5010 | FDA UDI | Class II | Active |
| Medical Science Products | PLB042-3016 | FDA UDI | Class II | Active |
| Relief Medical | PLB043-0400 | FDA UDI | Class II | Active |
| TheraKnit | TKP-3050 | FDA UDI | Class II | Active |
| Relief Medical | PLB043-3050 | FDA UDI | Class II | Active |
| ReBuilder Medical | PLB033-0818 | FDA UDI | Class II | Active |
| TheraKnit | TKG-3016 | FDA UDI | Class II | Active |
| TheraKnit | TKG-3026 | FDA UDI | Class II | Active |
| Relief Medical | PLB043-2030 | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-3020C | FDA UDI | Class II | Active |
| PDC Restorer | PLB066-1080 | FDA UDI | Class II | Active |
| Tn-28 | TKT-5002 | FDA UDI | Class II | Active |
| TheraKnit | TKG-3024 | FDA UDI | Class II | Active |
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