Data / Medical devices / Canada / National Therapy Products Inc.
National Therapy Products Inc.: FDA-registered device maker in Brampton Ontario, Canada, 2 510(k) clearances
National Therapy Products Inc. is registered with the FDA (registration 9710388) in Brampton Ontario, Canada. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 25, 2002. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 9710388
- FEI number
- 3003445500
- Address
- 420 Deerhurst Drive Unit 3, Brampton Ontario, Canada, L6T 5H9
- Owner or operator
- NATIONAL THERAPY PRODUCTS INC. (9046603)
- Roles
- Manufacturer
- First device listed
- May 5, 2008
- Registered through
- 2026
- Brand names listed
- Wavelength
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Media, Coupling, Ultrasound | MUI | 2 | Manufacturer | accessdata.fda.gov |
| Transducer, Ultrasonic, Diagnostic | ITX | 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 |
|---|---|---|---|---|---|---|
| February 25, 2002 | K013212 | WAVELENGHT ULTRASOUND LOTION | MUI | Substantially Equivalent | National Therapy Products, Inc. | accessdata.fda.gov |
| October 18, 2001 | K012522 | WAVELENGTH MULTI-PURPOSE ULTRASOUND GEL | ITX | Substantially Equivalent | National Therapy Products, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 25, 2002. 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.