Data / Medical devices / Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety / United States
FDA-registered makers of Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety in the United States: 7 establishments
7 establishments in the United States are registered with the FDA to make Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety (product code QJQ). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety
- Product code
- QJQ
- Country
- United States
Makers of Cranial Electrotherapy Stimulator To Treat Insomnia And/Or Anxiety in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| FISHER WALLACE LABORATORIES Inc | Brooklyn, NY, United States | Specification developer | 2 | October 4, 1990 | 0 | 1 | 0 | api.fda.gov |
| Electromedical Products Intl., Inc. | Mineral Wells, TX, United States | Manufacturer, Specification developer | 1 | May 12, 1992 | 0 | 0 | 0 | api.fda.gov |
| Neuro-Fitness LLC | Fall City, WA, United States | Specification developer | 1 | April 5, 2007 | 0 | 0 | 0 | api.fda.gov |
| Neurofield, Inc. | Santa Barbara, CA, United States | Complaint file establishment, Specification developer | 1 | December 31, 2025 | 0 | 0 | 0 | api.fda.gov |
| Nexalin Technology, Inc. | Houston, TX, United States | Complaint file establishment, Specification developer | 1 | July 21, 2003 | 0 | 0 | 0 | api.fda.gov |
| Apical Instruments | Redwood City, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Morgan Newton Company | Plano, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.