Data / Medical devices / Device, Nerve Conduction Velocity Measurement / United States
FDA-registered makers of Device, Nerve Conduction Velocity Measurement in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Device, Nerve Conduction Velocity Measurement (product code JXE). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Device, Nerve Conduction Velocity Measurement
- Product code
- JXE
- Country
- United States
Makers of Device, Nerve Conduction Velocity Measurement in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Rhythmlink International, LLC | Columbia, SC, United States | Manufacturer, Repackager or relabeler, Specification developer | 2 | October 5, 1992 | 0 | 0 | 0 | api.fda.gov |
| The Electrode Store | Buckley, WA, United States | Manufacturer | 1 | August 12, 2004 | 0 | 0 | 0 | api.fda.gov |
| Ad-Tech Medical Instrument Corp. | Oak Creek, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cadwell Industries, Inc. | Kennewick, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cirtec Medical | Brooklyn Park, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ducommun LaBarge Technologies | Appleton, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Laborie Medical Technologies Corp. | Portsmouth, NH, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nihon Kohden America, Inc. | Irvine, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Natus Neurology Incorporated | Middleton, WI, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Soterix Medical,inc. | Woodbridge, NJ, 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.