Data / Medical devices / Platform, Force-Measuring
Platform, Force-Measuring (KHX): 28 FDA-registered makers in 10 countries
28 establishments in 10 countries are registered with the FDA to make Platform, Force-Measuring (product code KHX, Class 1, 21 CFR 890.1575). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 15 510(k) clearances under this code, the latest on August 11, 1995, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- KHX
- Device class
- 1
- Regulation
- 890.1575
- Medical specialty
- Physical Medicine
Makers by country
| Country | Makers |
|---|---|
| United States | 13 |
| Italy | 3 |
| Germany | 3 |
| South Korea | 2 |
| France | 2 |
| China | 1 |
| Greece | 1 |
| Sweden | 1 |
| Poland | 1 |
| Canada | 1 |
Makers of Platform, Force-Measuring
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 |
|---|---|---|---|---|---|---|---|---|
| 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 | |
| BTS SPA | VIGONZA Padova, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diers International GMBH | Mainz-Kastel Hesse, Germany | Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Domino S.R.L. | Codogne Treviso, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diversified Healthcare Development LLC. | Independence, VA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dynamic solution Co., Ltd | Seongnam-si Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fourier Intelligence Inc. | Shanghai, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HTS, Inc. | Gold Canyon, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| InBody Co, Ltd. | Cheonan-si Chungnam, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kinvent Biomecanique | Montepellier Herault, France | Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kinvent Hellas | Thermi Kentriki Makedonia, Greece | Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Meloq AB | Stockholm, Sweden | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orthotic Holdings Inc. | Mesa, AZ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ottobock SE & Co. KGaA formerly known as Otto Bock Healthcare GmbH | DUDERSTADT Lower Saxony, Germany | Manufacturer | 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 | |
| Sensor Medica Srl | Guidonia Montecelio Roma, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sport Medical Technology Inc | Shirley, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Technomex | Gliwice Slaskie, Poland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Orthotic Group Inc. | Markham Ontario, Canada | Specification developer | 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 | |
| Virtualis | Montpellier Herault, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zebris Medical GMBH | Isny Baden-Wurttemberg, Germany | 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 August 11, 1995. 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.