Data / Medical devices / System, Isokinetic Testing And Evaluation / United States
FDA-registered makers of System, Isokinetic Testing And Evaluation in the United States: 19 establishments
19 establishments in the United States are registered with the FDA to make System, Isokinetic Testing And Evaluation (product code IKK). 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
- System, Isokinetic Testing And Evaluation
- Product code
- IKK
- Country
- United States
Makers of System, Isokinetic Testing And Evaluation in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Assistive Technology Development, Inc. | Orange, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Barrett Technology, LLC | Newton, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bertec Corp. | Columbus, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioness Medical, Inc. | Valencia, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bte Technologies | Hanover, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioventus LLC | Cordova, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Computer Sports Medicine, Inc. | Stoughton, MA, United States | Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Djo, LLC | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Figur8, Inc. | Boston, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Healing Innovations | Nashville, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medhab, LLC | Arlington, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mirus, LLC | Marietta, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Modus Health, LLC | Mountlake Ter, WA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Perry Dynamics, Inc. | Decatur, IL, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ROM Technologies, Inc. | Brookfield, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smart Machines Corporation | Medfield, MA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STS Corporation | Duluth, GA, United States | Complaint file establishment, Repackager or relabeler, 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 | |
| Verve Precision Measurement Inc | Arvada, CO, United States | Complaint file establishment, Repackager or relabeler, 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.