Data / Medical devices / Stimulator, Electrical, Transcutaneous, For Arthritis / United States
FDA-registered makers of Stimulator, Electrical, Transcutaneous, For Arthritis in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Stimulator, Electrical, Transcutaneous, For Arthritis (product code NYN). 2 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, Electrical, Transcutaneous, For Arthritis
- Product code
- NYN
- Country
- United States
Makers of Stimulator, Electrical, Transcutaneous, For Arthritis in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| VQ Orthocare | Vista, CA, United States | Complaint file establishment, Manufacturer | 2 | December 5, 2005 | 0 | 0 | 0 | api.fda.gov |
| Artheon Orthopedic Devices | La Verne, CA, United States | Specification developer | 1 | November 10, 2011 | 0 | 0 | 0 | api.fda.gov |
| Bear Down Brands, LLC | Fullerton, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Djo, LLC | Carlsbad, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hollywog, LLC | Chattanooga, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| KL Distributing | Hudson, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Manamed LLC | Denton, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pdi Works, LLC | Cleveland, TN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Theragen, Inc. | Jacksonville, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Twin River Group | Trenton, 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.