Data / Medical devices / Device, Iontophoresis, Other Uses / United States
FDA-registered makers of Device, Iontophoresis, Other Uses in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Device, Iontophoresis, Other Uses (product code EGJ). 7 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
- Device, Iontophoresis, Other Uses
- Product code
- EGJ
- Country
- United States
Makers of Device, Iontophoresis, Other Uses 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 | Specification developer | 16 | November 16, 2007 | 0 | 0 | 0 | api.fda.gov |
| North Coast Medical, Inc. | Morgan Hill, CA, United States | Manufacturer | 4 | February 13, 2014 | 0 | 0 | 0 | api.fda.gov |
| WR Medical Electronics Co. | Maplewood, MN, United States | Manufacturer | 3 | August 9, 2000 | 0 | 0 | 0 | api.fda.gov |
| Axelgaard MFG. Co., Ltd. | Fallbrook, CA, United States | Manufacturer | 1 | June 18, 2008 | 0 | 0 | 0 | api.fda.gov |
| General Medical Co. | Jacksonville, FL, United States | Complaint file establishment, Manufacturer | 1 | July 19, 1983 | 0 | 0 | 0 | api.fda.gov |
| LTS Therapy Systems, LLC | West St Paul, MN, United States | Manufacturer | 1 | February 1, 2000 | 0 | 2 | 0 | api.fda.gov |
| Soterix Medical,inc. | Woodbridge, NJ, United States | Manufacturer | 1 | May 1, 2017 | 0 | 0 | 0 | api.fda.gov |
| Clearlake-Tech Inc | Clear Lake, SD, United States | Contract manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cardinal Health | Wabasha, MN, 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.