Data / Medical devices / Stimulator, Nerve, Transcutaneous, Over-The-Counter / United States
FDA-registered makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter in the United States: 35 establishments
35 establishments in the United States are registered with the FDA to make Stimulator, Nerve, Transcutaneous, Over-The-Counter (product code NUH). 30 have 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
- Stimulator, Nerve, Transcutaneous, Over-The-Counter
- Product code
- NUH
- Country
- United States
Makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bear Down Brands, LLC | Fullerton, CA, United States | Complaint file establishment, Specification developer | 5 | May 13, 2023 | 0 | 0 | 0 | api.fda.gov |
| Djo, LLC | Carlsbad, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 4 | July 1, 2020 | 0 | 0 | 0 | api.fda.gov |
| Hinge Health Inc. | San Francisco, CA, United States | Complaint file establishment, Specification developer | 2 | February 23, 2024 | 0 | 0 | 0 | api.fda.gov |
| Prizm Medical, Inc. | Buford, GA, United States | Manufacturer | 2 | December 3, 2014 | 0 | 0 | 0 | api.fda.gov |
| Alc Enterprises Inc | Brooklyn, NY, United States | Specification developer | 1 | December 2, 2019 | 0 | 0 | 0 | api.fda.gov |
| Avazzia, Inc. | Dallas, TX, United States | Complaint file establishment, Manufacturer | 1 | May 12, 2017 | 0 | 0 | 0 | api.fda.gov |
| BioMedical Life Systems Inc. | Carlsbad, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 1 | July 29, 2011 | 0 | 0 | 0 | api.fda.gov |
| Chek Medical | Aurora, CO, United States | Repackager or relabeler, Specification developer | 1 | March 25, 2021 | 0 | 0 | 0 | api.fda.gov |
| Chirp Innovation, LLC | Lehi, UT, United States | Complaint file establishment, Specification developer | 1 | June 27, 2024 | 0 | 0 | 0 | api.fda.gov |
| Digicom Electronics, Inc. | Oakland, CA, United States | Manufacturer | 1 | November 21, 2015 | 0 | 0 | 0 | api.fda.gov |
| Dynapulse Medical LLC | Minnetonka, MN, United States | Specification developer | 1 | December 23, 2025 | 0 | 0 | 0 | api.fda.gov |
| Drive Northpoint, LLC | Palmetto, GA, United States | Manufacturer | 1 | September 16, 2013 | 0 | 0 | 0 | api.fda.gov |
| Electronic Waveform Lab, Inc. | Huntingtn Bch, CA, United States | Manufacturer | 1 | September 15, 2016 | 0 | 0 | 0 | api.fda.gov |
| Fashionable, Inc. | Largo, FL, United States | Complaint file establishment, Specification developer | 1 | December 2, 2019 | 0 | 0 | 0 | api.fda.gov |
| Global TV Concepts, Ltd. | Coconut Creek, FL, United States | Specification developer | 1 | November 12, 2014 | 0 | 0 | 0 | api.fda.gov |
| Hollywog, LLC | Chattanooga, TN, United States | Manufacturer | 1 | September 22, 2017 | 0 | 0 | 0 | api.fda.gov |
| KL Distributing | Hudson, FL, United States | Manufacturer | 1 | June 21, 2019 | 0 | 0 | 0 | api.fda.gov |
| Laser Health Technologies | Paradise Valley, AZ, United States | Repackager or relabeler, Specification developer | 1 | April 15, 2010 | 0 | 0 | 0 | api.fda.gov |
| Manamed LLC | Denton, TX, United States | Specification developer | 1 | November 3, 2023 | 0 | 0 | 0 | api.fda.gov |
| Marc Pro, Inc. | Huntington Beach, CA, United States | Specification developer | 1 | January 24, 2014 | 0 | 0 | 0 | api.fda.gov |
| Med International Inc | Ontario, CA, United States | Specification developer | 1 | July 21, 2015 | 0 | 0 | 0 | api.fda.gov |
| Micro Current Technology, Inc. | Seattle, WA, United States | Manufacturer | 1 | March 1, 2024 | 0 | 0 | 0 | api.fda.gov |
| Neurometrix, Inc. | Rockaway, NJ, United States | Manufacturer | 1 | January 5, 2016 | 0 | 0 | 0 | api.fda.gov |
| North Coast Medical, Inc. | Morgan Hill, CA, United States | Manufacturer | 1 | June 7, 2018 | 0 | 0 | 0 | api.fda.gov |
| Pdi Works, LLC | Cleveland, TN, United States | Specification developer | 1 | March 1, 2012 | 0 | 0 | 0 | api.fda.gov |
| Pixie Cup LLC | Walnut Shade, MO, United States | Specification developer | 1 | August 12, 2024 | 0 | 0 | 0 | api.fda.gov |
| Pourang Bral, DDS, LLC | Jersey City, NJ, United States | Manufacturer | 1 | July 9, 2022 | 0 | 0 | 0 | api.fda.gov |
| Twin River Group | Trenton, NJ, United States | Manufacturer | 1 | November 9, 2018 | 0 | 0 | 0 | api.fda.gov |
| Transtimulation Research Inc | Pasadena, CA, United States | Manufacturer | 1 | April 9, 2025 | 0 | 0 | 0 | api.fda.gov |
| XF Agencija US Inc. | Chicago, IL, United States | Specification developer | 1 | December 2, 2019 | 0 | 0 | 0 | api.fda.gov |
| Heat In A Click LLC | Dania, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Krenerb, LLC | Hockessin, DE, United States | Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orchid Orthopedic Solutions Alabama LLC | Arab, AL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sonic Manufacturing Technologies, Inc. | Fremont, CA, 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 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.