Data / Medical devices / Holder, Crutch And Cane, Wheelchair / United States
FDA-registered makers of Holder, Crutch And Cane, Wheelchair in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Holder, Crutch And Cane, Wheelchair (product code IMZ). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Holder, Crutch And Cane, Wheelchair
- Product code
- IMZ
- Country
- United States
Makers of Holder, Crutch And Cane, Wheelchair in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| ASP Global, LLC | Austell, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Invacare Corp. Dba Invacare America | N Ridgeville, OH, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Onlycare Inc | Denver, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pride Mobility Products Corp. | North Las Vegas, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pride Mobility Products Corp. | Duryea, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pride Mobility Products Corporation | North Las Vegas, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reachable Technology | Cambridge, MA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stealth Products | Burnet, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sunrise Medical (us) LLC | Fresno, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sunrise Medical (US) LLC | Mount Juliet, TN, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.