Data / Medical devices / Canada / PDG Product Design Group, Inc.
PDG Product Design Group, Inc.: FDA-registered device maker in Richmond British Columbia, Canada, 5 510(k) clearances
PDG Product Design Group, Inc. is registered with the FDA (registration 9681827) in Richmond British Columbia, Canada. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated January 17, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9681827
- FEI number
- 3003748905
- Address
- 14273 Knox Way Unit 138, Richmond British Columbia, Canada, V6V 2Z4
- Owner or operator
- Permobil Inc (9025865)
- Roles
- Manufacturer
- First device listed
- August 15, 1996
- Registered through
- 2026
- Brand names listed
- BENTLEY, BENTLEY LT-R, BENTLEY LT, ECLIPSE, Eclipse 350, FUZE T50N, FUZE JR, FUZE M50, FUZE T50, STELLAR GLT. STELLAR IMPACT, STELLAR HD, STELLAR GL, Wheelchair Accessories
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Manufacturer | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | 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 |
|---|---|---|---|---|---|---|
| January 17, 2007 | K063736 | FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50 | IOR | Substantially Equivalent | Pdg Product Design Group, Inc. | accessdata.fda.gov |
| March 22, 1999 | K990557 | THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR | IOR | Substantially Equivalent | Pdg Product Design Group, Inc. | accessdata.fda.gov |
| May 9, 1997 | K971389 | ECLIPSE 400 MANUALLY OPERATED WHEELCAIR | IOR | Substantially Equivalent | Pdg Product Design Group, Inc. | accessdata.fda.gov |
| February 14, 1997 | K970311 | BENTLEY MANUALLY OPERATED WHEELCHAIR | IOR | Substantially Equivalent | Pdg Product Design Group, Inc. | accessdata.fda.gov |
| May 29, 1996 | K961743 | ECLIPSE 600 MANUALLY OPERATED WHEELCHAIR | IOR | Substantially Equivalent | Pdg Product Design Group, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Wheelchair, Mechanical
- All makers of Accessories, Wheelchair
- All makers of Components, Wheelchair
Updated January 17, 2007. 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.