Data / Medical devices / Canada / Broda LP
Broda LP: FDA-registered device maker in Kitchener Ontario, Canada, 1 510(k) clearance
Broda LP is registered with the FDA (registration 8043392) in Kitchener Ontario, Canada. It lists 13 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 21, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8043392
- FEI number
- 3007074101
- Address
- 560 Bingemans Centre Dr, Kitchener Ontario, Canada, N2B3X9
- Owner or operator
- Broda LP (9001296)
- Roles
- Manufacturer
- First device listed
- June 5, 1996
- Registered through
- 2026
- Brand names listed
- (Broda LP), 89K-NN, 89K-NO, Traversa Transport Wheelchair
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Manufacturer | accessdata.fda.gov |
| Armrest, Wheelchair | IML | 1 | Manufacturer | accessdata.fda.gov |
| Attachment, Narrowing, Wheelchair | IMQ | 1 | Manufacturer | accessdata.fda.gov |
| Board, Lap, Wheelchair | IMX | 1 | Manufacturer | accessdata.fda.gov |
| Chair And Table, Medical | KMN | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Adjustable, Mechanical | INN | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Geriatric | FRJ | 1 | Manufacturer | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Manufacturer | accessdata.fda.gov |
| Device, Anti-Tip, Wheelchair | IMR | 1 | Manufacturer | accessdata.fda.gov |
| Footrest, Wheelchair | IMM | 1 | Manufacturer | accessdata.fda.gov |
| Restraint, Wheelchair, Non-Protective | KID | 1 | Manufacturer | accessdata.fda.gov |
| Support, Head And Trunk, Wheelchair | IMS | 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 |
|---|---|---|---|---|---|---|
| July 21, 2003 | K032133 | BRODA MODEL 587 MANUAL WHEELCHAIR | IOR | Substantially Equivalent | Broda Ent., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Components, Wheelchair
- All makers of Board, Lap, Wheelchair
- All makers of Accessories, Wheelchair
- All makers of Footrest, Wheelchair
- All makers of Wheelchair, Mechanical
- All makers of Support, Head And Trunk, Wheelchair
Updated July 21, 2003. 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.