Data / Medical devices / Canada / Universal Pain Technology Canada Inc.
Universal Pain Technology Canada Inc.: FDA-registered device maker in PRINCE GEORGE British Columbia, Canada, 1 510(k) clearance
Universal Pain Technology Canada Inc. is registered with the FDA (registration 3002654235) in PRINCE GEORGE British Columbia, Canada. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 27, 2005. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3002654235
- Address
- 1648 Ogilvie ST. South, PRINCE GEORGE British Columbia, Canada, V2N 1W9
- Owner or operator
- UNIVERSAL PAIN TECHNOLOGY CANADA INC. (9046648)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- July 11, 2001
- Registered through
- 2027
- Brand names listed
- MANU HAND BRACE, SpineMED Express Cervical Decompression System, SpineMED Express Decompression System, SpineMED Professional Cervical Decompression System, SpineMED Professional Decompression System, SpineMED Ultra Cervical Decompression System, SpineMED Ultra Decompression System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Equipment, Traction, Powered | ITH | 2 | Manufacturer | accessdata.fda.gov |
| Orthosis, Limb Brace | IQI | 1 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| April 27, 2005 | K051013 | SPINEMED S200B/S200C | ITH | Substantially Equivalent | Cert Health Sciences, LLC | accessdata.fda.gov |
Compare with other makers
Updated April 27, 2005. 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.