Data / Medical devices / Exerciser, Non-Measuring For Stroke Rehabilitation / United States
FDA-registered makers of Exerciser, Non-Measuring For Stroke Rehabilitation in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Exerciser, Non-Measuring For Stroke Rehabilitation (product code PKS). 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
- Exerciser, Non-Measuring For Stroke Rehabilitation
- Product code
- PKS
- Country
- United States
Makers of Exerciser, Non-Measuring For Stroke Rehabilitation in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Accelerated Care Plus Corp. | Reno, NV, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bodypoint Designs, Inc. | Seattle, WA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mirrored Motion Works Inc | Durham, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neuro Rehab Recovery Inc | Belleair, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Resola | Idaho Falls, ID, United States | 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.