Data / Medical devices / Canada / Thought Technology Ltd.
Thought Technology Ltd.: FDA-registered device maker in MONTREAL Quebec, Canada, 10 510(k) clearances
Thought Technology Ltd. is registered with the FDA (registration 9680487) in MONTREAL Quebec, Canada. It lists 5 device types. The FDA files 10 510(k) clearances under its listings, the newest dated June 17, 2022. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 9680487
- FEI number
- 1000639819
- Address
- 5250 Ferrier Suite 812, MONTREAL Quebec, Canada, H4P 1L3
- Owner or operator
- THOUGHT TECHNOLOGY LTD. (9009398)
- Roles
- Manufacturer, Specification developer
- First device listed
- February 2, 1994
- Registered through
- 2027
- Brand names listed
- 100 Triodes AG/AGCL, 4100 - EMG-EZ Device (60Hz), 4120 - EMG-EZ Device (50Hz), 5031A0011 - Venus Clinic Encoder, 5150M0011 - Venus Clinic SW User Manual, 5150M0021 - Venus Clinic HW User Guide, 5150M0031 - Venus Clinic Installation Guide, 6W, 5V, Multiplug Medical Power Supply and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Biofeedback | HCC | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Perineometer | HIR | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Electrical, Non-Implantable, For Incontinence | KPI | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 17, 2022 | K213197 | MyOnyx System | IPF | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| January 13, 2021 | K201014 | MyOnyx System | KPI | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| March 15, 2006 | K053434 | MYOTRAC INFINITI ELECTRICAL STIMULATOR | KPI | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| December 29, 2005 | K053266 | MYOTRAC INFINITI | IPF | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| October 2, 1997 | K972723 | BIO TROL | HCC | Substantially Equivalent | Mindmedia Labs, Inc. | accessdata.fda.gov |
| September 29, 1995 | K925681 | MYOTRAC2D/CS | HIR | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| May 11, 1995 | K935213 | INCONTROL | HIR | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| May 11, 1995 | K932149 | THOUGHT TECHNOLOGY VAGINAL & RECTAL ELECTRODE | HIR | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| February 12, 1991 | K903497 | FLEXCOMP DSP & PROCOMP | HCC | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
| September 26, 1988 | K881416 | MYOTRAC | HCC | Substantially Equivalent | Thought Technology , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Biofeedback
- All makers of Perineometer
- All makers of Stimulator, Muscle, Powered
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Stimulator, Electrical, Non-Implantable, For Incontinence
Updated June 17, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.