Data / Medical devices / Goniometer, Ac-Powered / United States
FDA-registered makers of Goniometer, Ac-Powered in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Goniometer, Ac-Powered (product code KQX). 1 has 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
- Goniometer, Ac-Powered
- Product code
- KQX
- Country
- United States
Makers of Goniometer, Ac-Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Djo, LLC | Carlsbad, CA, United States | Specification developer | 1 | November 28, 1994 | 0 | 0 | 0 | api.fda.gov |
| Activbody | San Diego, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arthrex, Inc. | Naples, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioniks | Alameda, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Canary Medical Usa LLC | Carlsbad, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Electronic Technologies LLC | New Hope, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| JTECH Medical Industries, Inc. | Midvale, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lafayette Instrument Co., Inc. | La Fayette, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Maxx Orthopedics Inc. | Norristown, PA, United States | Manufacturer, Remanufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medhab, LLC | Arlington, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Motive Health, Inc. | Tempe, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Noraxon Usa, Inc. | Scottsdale, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| NeckCare Enterprises, Inc | Minneapolis, MN, United States | Complaint file establishment, Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ROM Technologies, Inc. | Brookfield, CT, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Synapse Biomedical Inc. | Oberlin, OH, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Titronics Research & Development | Tiffin, IA, United States | Manufacturer | 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.