Data / Medical devices / Platform, Force-Measuring / United States
FDA-registered makers of Platform, Force-Measuring in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Platform, Force-Measuring (product code KHX). 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
- Platform, Force-Measuring
- Product code
- KHX
- Country
- United States
Makers of Platform, Force-Measuring in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Advanced Mechanical Technology Inc | Watertown, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Balance Tracking Systems Incorporated | San Diego, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bertec Corp. | Columbus, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diversified Healthcare Development LLC. | Independence, VA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HTS, Inc. | Gold Canyon, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orthotic Holdings Inc. | Mesa, AZ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Performance Health Systems, LLC | Northbrook, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pivot - Edm | La Vista, NE, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pivot International | Lenexa, KS, 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 | |
| Turner Imaging Systems, Inc. | Orem, UT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Uprightvr Inc. | Bel Air, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zibrio, Inc | Houston, TX, United States | Complaint file establishment, 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.