Data / Medical devices / Walker, Mechanical / United States
FDA-registered makers of Walker, Mechanical in the United States: 46 establishments
46 establishments in the United States are registered with the FDA to make Walker, Mechanical (product code ITJ). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Walker, Mechanical
- Product code
- ITJ
- Country
- United States
Makers of Walker, Mechanical in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Amarigo Inc | Los Angeles, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Agiliti Health - Hays | Hays, KS, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Apricity | Appleton, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Blickman Industries LLC | Lawrenceburg, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Brownmed | Spirit Lake, IA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Core Mobility Solutions | Los Gatos, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Camino Robotics, Inc. | Torrance, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Community Products, LLC | Rifton, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Djo, LLC | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Drive Northpoint, LLC | Palmetto, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ekso Bionics | San Rafael, CA, 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 | |
| Exokinetics, Inc. | West Chester, PA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Enliten LLC | Newark, DE, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Evolution Technologies USA Inc. | Ferndale, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| First Nation Group, LLC | Saint Petersburg, FL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Freedom To Roam, LLC | Windsor Heights, IA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GF Health Products, Inc. | Fond du Lac, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Healthline Medical Products | Winter Garden, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Helavo Corporation | Miami, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hill-Rom, Inc. | Batesville, IN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Horst Enterprises Inc | Saint Petersburg, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| In-Step Mobility Products Corporation | Skokie, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Innomotive LLC | East Lansing, MI, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Innovative Products Unlimited, Inc. | Niles, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kismet Holdings Group | Hixson, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mediterry Inc. | Tamaroa, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Merchsource LLC | Irvine, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mor-Medical International | Pharr, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medegen Medical Products | Gallaway, TN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mobility Research | Phoenix, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Noka Medical Inc | City Of Industry, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| P.C.P. Champion | Ripley, OH, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phoenix Medical Solutions | Hunt Valley, MD, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Prime Engineering | Fresno, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Secured Ortho Manufacturing Of America, LLC | Deer Park, NY, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Span Link International LLC | Deer Park, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stander, Inc | Logan, UT, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sport Medical Technology Inc | Shirley, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sunrise Medical (US) LLC | Mount Juliet, TN, United States | Complaint file establishment, Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Knee Walker Company Inc | Altamonte Springs, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Top Shelf Manufacturing, LLC | Tracy, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Transparent Supply Solutions Ltd. | Dover, DE, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Unite Medical, LLC | Lithia Springs, GA, United States | 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.