Data / Medical devices / Stimulator, Nerve, Transcutaneous, For Pain Relief / United States
FDA-registered makers of Stimulator, Nerve, Transcutaneous, For Pain Relief in the United States: 56 establishments
56 establishments in the United States are registered with the FDA to make Stimulator, Nerve, Transcutaneous, For Pain Relief (product code GZJ). 29 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.
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- Device
- Stimulator, Nerve, Transcutaneous, For Pain Relief
- Product code
- GZJ
- Country
- United States
Makers of Stimulator, Nerve, Transcutaneous, For Pain Relief 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 | Manufacturer, Specification developer | 5 | June 3, 2016 | 0 | 0 | 0 | api.fda.gov |
| Biowave Corporation | Norwalk, CT, United States | Manufacturer, Specification developer | 4 | February 24, 2021 | 0 | 0 | 0 | api.fda.gov |
| BioMedical Life Systems Inc. | Carlsbad, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 4 | July 26, 2006 | 0 | 0 | 0 | api.fda.gov |
| ReliefBand Technologies | Horsham, PA, United States | Complaint file establishment, Specification developer | 4 | August 30, 2019 | 0 | 0 | 0 | api.fda.gov |
| Electrostim Medical Services, Inc. | Tampa, FL, United States | Specification developer | 3 | May 8, 2009 | 0 | 0 | 0 | api.fda.gov |
| Integrated Biomedical Corp. | Las Vegas, NV, United States | Manufacturer | 3 | February 2, 1990 | 0 | 0 | 0 | api.fda.gov |
| Avazzia, Inc. | Dallas, TX, United States | Complaint file establishment, Manufacturer | 2 | May 23, 2014 | 0 | 1 | 0 | api.fda.gov |
| Electronic Waveform Lab, Inc. | Huntingtn Bch, CA, United States | Manufacturer, Specification developer | 2 | December 6, 2011 | 0 | 0 | 0 | api.fda.gov |
| Mettler Electronics Corp. | Anaheim, CA, United States | Manufacturer, Repackager or relabeler | 2 | December 10, 2003 | 0 | 0 | 0 | api.fda.gov |
| Micro Current Technology, Inc. | Seattle, WA, United States | Manufacturer | 2 | October 21, 2003 | 0 | 0 | 0 | api.fda.gov |
| ReBuilder Medical, Inc. | Charles Town, WV, United States | Manufacturer | 2 | April 24, 1989 | 0 | 0 | 0 | api.fda.gov |
| Theragen, Inc. | Jacksonville, FL, United States | Specification developer | 2 | January 9, 2012 | 0 | 0 | 0 | api.fda.gov |
| Truerelief | Scottsdale, AZ, United States | Complaint file establishment, Manufacturer, Specification developer | 2 | March 23, 2021 | 0 | 0 | 0 | api.fda.gov |
| Algiamed Technologies Usa Inc | Lake Mary, FL, United States | Manufacturer | 1 | January 18, 2017 | 0 | 0 | 0 | api.fda.gov |
| Altivera Medical, Inc. | Englewood, CO, United States | Manufacturer | 1 | August 27, 2024 | 0 | 0 | 0 | api.fda.gov |
| Bio-Research Associates, Inc. | Mequon, WI, United States | Complaint file establishment, Manufacturer | 1 | August 28, 2006 | 0 | 0 | 0 | api.fda.gov |
| Calmare Therapeutics Incorporated | Shelton, CT, United States | Manufacturer | 1 | February 20, 2009 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 1 | July 31, 1996 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Wabasha, MN, United States | Contract manufacturer, Manufacturer | 1 | July 31, 1996 | 0 | 0 | 0 | api.fda.gov |
| Digicom Electronics, Inc. | Oakland, CA, United States | Manufacturer | 1 | February 13, 2007 | 0 | 0 | 0 | api.fda.gov |
| Drive Northpoint, LLC | Palmetto, GA, United States | Manufacturer, Repackager or relabeler | 1 | November 27, 2007 | 0 | 0 | 0 | api.fda.gov |
| Electromedical Products Intl., Inc. | Mineral Wells, TX, United States | Manufacturer, Specification developer | 1 | February 23, 1990 | 0 | 0 | 0 | api.fda.gov |
| Electromedical Technologies, Inc | Scottsdale, AZ, United States | Manufacturer, Specification developer | 1 | July 6, 2007 | 0 | 0 | 0 | api.fda.gov |
| FISHER WALLACE LABORATORIES Inc | Brooklyn, NY, United States | Specification developer | 1 | April 10, 1990 | 0 | 0 | 0 | api.fda.gov |
| Inspirstar, Inc. | Chandler, AZ, United States | Specification developer | 1 | March 14, 2006 | 0 | 0 | 0 | api.fda.gov |
| InterX Technologies | Plano, TX, United States | Manufacturer, Repackager or relabeler | 1 | May 17, 2005 | 0 | 1 | 0 | api.fda.gov |
| Laser Health Technologies | Paradise Valley, AZ, United States | Repackager or relabeler, Specification developer | 1 | May 6, 2009 | 0 | 0 | 0 | api.fda.gov |
| Neurological Fitness Equipment And Education LLC | Austin, TX, United States | Complaint file establishment, Manufacturer, Repackager or relabeler | 1 | February 2, 2001 | 0 | 0 | 0 | api.fda.gov |
| Z Technologies, LLC | Atlanta, GA, United States | Manufacturer | 1 | August 27, 1997 | 0 | 0 | 0 | api.fda.gov |
| AB Electronics | Danbury, CT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Accelerated Care Plus Corp. | Reno, NV, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Amrex-Zetron, Inc. | Paramount, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ascentron, Inc. | White City, OR, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Clearlake-Tech Inc | Clear Lake, SD, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Creation Technologies | Newark, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Distron Corporation | Attleboro Falls, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dynapulse Medical LLC | Minnetonka, MN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Imex, LLC | Fulton, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| J Sterling Industries LLC | Kalamazoo, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jomel Seams Reasonable LLC | Hillside, NJ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| KL Distributing | Hudson, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Liberty Medical Solutions, LLC | Tampa, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Manamed LLC | Denton, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Quant Usa | Solon, OH, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Morgan Newton Company | Plano, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Motive Health, Inc. | Tempe, AZ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neurolumen LLC | Oklahoma City, OK, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Preferred Depot | Irvine, CA, United States | Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Prizm Medical, Inc. | Buford, GA, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pivot International | Lenexa, KS, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rst-Sanexas | Henderson, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spectrum Assembly Inc. | Carlsbad, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Svtronics, Inc. | Plano, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Systec Engineering, LLC | Euless, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sanbor Medical | Allentown, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Therabody, Inc. | Los Angeles, CA, United States | Complaint file establishment, Specification developer | 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.