Data / Medical devices / Interactive Rehabilitation Exercise Devices
Interactive Rehabilitation Exercise Devices (LXJ): 9 FDA-registered makers in 6 countries
9 establishments in 6 countries are registered with the FDA to make Interactive Rehabilitation Exercise Devices (product code LXJ, Class 2, 21 CFR 890.5360). 9 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 27 510(k) clearances under this code, the latest on October 10, 2019, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- LXJ
- Device class
- 2
- Regulation
- 890.5360
- Medical specialty
- Physical Medicine
Makers by country
| Country | Makers |
|---|---|
| United States | 3 |
| Canada | 2 |
| Italy | 1 |
| Switzerland | 1 |
| Sweden | 1 |
| United Kingdom | 1 |
Makers of Interactive Rehabilitation Exercise Devices
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| BTS SPA | VIGONZA Padova, Italy | Manufacturer | 1 | April 17, 2014 | 0 | 0 | 0 | api.fda.gov |
| Cadwell Industries, Inc. | Kennewick, WA, United States | Manufacturer, Specification developer | 1 | June 1, 1993 | 0 | 0 | 0 | api.fda.gov |
| Emovi Inc. | Montreal Quebec, Canada | Complaint file establishment, Manufacturer | 1 | October 26, 2009 | 0 | 0 | 0 | api.fda.gov |
| Jintronix Inc. | Montreal Quebec, Canada | Manufacturer | 1 | April 22, 2015 | 0 | 0 | 0 | api.fda.gov |
| NeuroXtherapeutics SA | Lausanne Vaud, Switzerland | Repackager or relabeler, Specification developer | 1 | April 24, 2017 | 0 | 0 | 0 | api.fda.gov |
| Qualisys AB | Goteborg Vastra Gotaland, Sweden | Manufacturer | 1 | August 2, 2018 | 0 | 0 | 0 | api.fda.gov |
| Scientific Analytics/DARI Motion, Overland Park, KS USA | Overland Park, KS, United States | Manufacturer | 1 | March 7, 2019 | 0 | 0 | 0 | api.fda.gov |
| Vicon Motion Systems Inc | Centennial, CO, United States | Complaint file establishment, Specification developer | 1 | June 16, 1981 | 0 | 0 | 0 | api.fda.gov |
| Vicon Motion Systems, Ltd. | YARNTON Oxfordshire, United Kingdom | Manufacturer | 1 | June 16, 1981 | 0 | 0 | 0 | api.fda.gov |
Updated October 10, 2019. 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.