Data / Medical devices / Canada / Center For Pain And Stress Research, Ltd.
Center For Pain And Stress Research, Ltd.: FDA-registered device maker in TORONTO Ontario, Canada, 2 510(k) clearances
Center For Pain And Stress Research, Ltd. is registered with the FDA (registration 3002669614) in TORONTO Ontario, Canada. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 4, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002669614
- Address
- 3679a Lakeshore BLVD West, TORONTO Ontario, Canada, M8W 1P7
- Owner or operator
- CENTER FOR PAIN AND STRESS RESEARCH, LTD. (9025652)
- Roles
- Manufacturer
- First device listed
- June 23, 2003
- Registered through
- 2026
- Brand names listed
- Dolphin Neurostim, Dolphin Neurostim OTC, Dolphin Neurostim Professional, Dolphin Neurostim Professional OTC
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 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 |
|---|---|---|---|---|---|---|
| March 4, 2015 | K133789 | DOLPHIN NEUROSTIM OTC | NUH | Substantially Equivalent | Acumed Medical , Ltd. | accessdata.fda.gov |
| June 17, 2003 | K023726 | TENS PRO 900 | GZJ | Substantially Equivalent | Acumed Medical Supplies , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
Updated March 4, 2015. 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.