Data / Medical devices / Cane, Safety Walk / United States
FDA-registered makers of Cane, Safety Walk in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Cane, Safety Walk (product code KHY). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Cane, Safety Walk
- Product code
- KHY
- Country
- United States
Makers of Cane, Safety Walk in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alex Orthopedic, Inc. | Grand Prairie, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ergoactives, LLC | Miami, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Global TV Concepts, Ltd. | Coconut Creek, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Horst Enterprises Inc | Saint Petersburg, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Onlycare Inc | Denver, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SHOP LC Global Inc. | Austin, TX, United States | Contract manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.