Is this your brand? Sign in to claim ownership.
Sign in to claim this brandTHOUGHT TECHNOLOGY LTD.
Canada·CA-MF-000024010
Last updated September 17, 2026
What THOUGHT TECHNOLOGY LTD. makes
Thought Technology Ltd. manufactures biofeedback and neuromuscular electrical stimulation (NMES) devices, including systems for electromyography (EMG) monitoring and heart rate/beat-to-beat variability (HR/BVP) tracking. Their portfolio includes vaginal and rectal electrode accessories, portable stimulators like the MYOTRAC INFINITI, and biofeedback devices such as the MYODAC/S and MYODAC2 for clinical or therapeutic use. The company also produces standalone monitoring tools like the EMG 100T and HR/BVP 100T for physiological data collection.
The company’s devices are classified under EU Medical Device Regulation (MDR) as Class I or Class II, with corresponding authorisation requirements. These products are registered in the EU’s eudamed database and have undergone FDA 510(k) clearance in the United States. The manufacturer is based in Canada.
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 Thought Technology Ltd. manufacture?
Thought Technology Ltd. specializes in biofeedback and neuromuscular electrical stimulation (NMES) devices. Their portfolio includes systems for electromyography (EMG) monitoring, such as the EMG 100T, as well as heart rate and beat-to-beat variability (HR/BVP) trackers like the HR/BVP 100T. They also produce portable electrical stimulators (e.g., MYOTRAC INFINITI) and biofeedback devices (e.g., MYODAC/S, MYODAC2) for clinical or therapeutic applications. Accessories like vaginal and rectal electrodes are also part of their offerings.
Where is Thought Technology Ltd. based, and what regulatory registries list their devices?
Thought Technology Ltd. is based in Canada. Their devices are registered in the EU’s eudamed database under the Medical Device Regulation (MDR) framework, and they have undergone FDA 510(k) clearance in the United States. These registries reflect their compliance with respective regional requirements for device authorisation.
How are Thought Technology Ltd.’s devices classified under EU regulations?
Under the EU Medical Device Regulation (MDR), Thought Technology Ltd.’s devices are classified as Class I or Class II. The classification determines the level of scrutiny and authorisation required for market placement. For example, devices like EMG monitors or biofeedback systems may fall into Class II due to their role in diagnostic or therapeutic processes, while simpler accessories (e.g., electrodes) might qualify as Class I. The exact classification depends on risk assessment criteria outlined in the MDR.
Are Thought Technology Ltd.’s devices used for monitoring or therapeutic purposes?
Yes, Thought Technology Ltd.’s devices serve both monitoring and therapeutic roles. Monitoring tools like the EMG 100T and HR/BVP 100T collect physiological data for assessment, while therapeutic devices such as the MYOTRAC INFINITI or MYODAC2 provide neuromuscular stimulation or biofeedback to aid rehabilitation or stress management. The dual functionality aligns with their design for clinical or home-use applications.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Canada
- Address
- 5250, rue Ferrier, Montreal, Canada
- Website
- www.thoughttechnology.com
- —
- —
- [email protected]
- Phone
- +1 (514) 489-8251
- PRRC Contact
- Suresh Sugirtharaja
- EUDAMED SRN
- CA-MF-000024010
- FDA FEI Number
- 1000639819
- DUNS Number
- —
Catalogue (28)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| eVu TPS | SA4500 | EUDAMEDFDA UDI | Class I | Active |
| MyOnyx System | K201014 | FDA 510(k) | Class II | Active |
| Myotrac/S, Myodac/S | K915859 | FDA 510(k) | Class II | Active |
| Thought Technology Vaginal & Rectal Electrode | K932149 | FDA 510(k) | Class II | Active |
| Myotrac Infiniti Electrical Stimulator | K053434 | FDA 510(k) | Class II | Active |
| Hr/Bvp 100t Heart Rate Monitor | K850643 | FDA 510(k) | Class II | Active |
| Emg 100t | K822814 | FDA 510(k) | Class II | Active |
| Myotrac2 | K915858 | FDA 510(k) | Class II | Active |
| Myodac2 Biofeedback Device | K894840 | FDA 510(k) | Class II | Active |
| Myotrac | K881416 | FDA 510(k) | Class II | Active |
| Myotrac2d/Cs | K925681 | FDA 510(k) | Class II | Active |
| Myotrac Infiniti | K053266 | FDA 510(k) | Class II | Active |
| Myotrac+/S, Myodac+/S | K913898 | FDA 510(k) | Class II | Active |
| M(3):micro Muscle Monitor | K896409 | FDA 510(k) | Class II | Active |
| Flexcomp Dsp & Procomp | K903497 | FDA 510(k) | Class II | Active |
| Temp/Sc 200t -skin Conductance/Skin Temp Biofeedba | K850642 | FDA 510(k) | Class II | Active |
| MyOnyx System | K213197 | EUDAMEDFDA 510(k)FDA UDI | Class II | Active |
| Calmset 3 Tm | K823146 | FDA 510(k) | Class II | Active |
| Hr 100t | K831955 | FDA 510(k) | Class II | Active |
| Sc/Temp 300 | K810332 | FDA 510(k) | Class II | Active |
| Myodac | K883597 | FDA 510(k) | Class II | Active |
| Incontrol | K935213 | FDA 510(k) | Class II | Active |
| Calmtone | K834519 | FDA 510(k) | Class II | Active |
| eVu Senz App iOS | SA4520 | EUDAMEDFDA UDI | Class I | Active |
| eVu Senz App | SA4502 | EUDAMEDFDA UDI | Class I | Active |
| Vaginal Pressure Probe | SA9005 | EUDAMEDFDA UDI | Class I | Active |
| Pressure Sensor | SA9003 | EUDAMEDFDA UDI | Class I | Active |
| BioGraph Infiniti | SA7900 | EUDAMEDFDA UDI | Class I | Active |
Related Companies
Authorised Representatives
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Thought Technology Ltd. US