Data / Medical devices / Device, Iontophoresis, Specific Uses / United States
FDA-registered makers of Device, Iontophoresis, Specific Uses in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Device, Iontophoresis, Specific Uses (product code KTB). 3 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
- Device, Iontophoresis, Specific Uses
- Product code
- KTB
- Country
- United States
Makers of Device, Iontophoresis, Specific 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 | 6 | December 22, 2003 | 0 | 0 | 0 | api.fda.gov |
| ELITechGroup Inc | Logan, UT, United States | Manufacturer | 3 | July 27, 2018 | 0 | 0 | 0 | api.fda.gov |
| WR Medical Electronics Co. | Maplewood, MN, United States | Manufacturer | 1 | November 18, 1999 | 0 | 0 | 0 | api.fda.gov |
| Amrex-Zetron, Inc. | Paramount, CA, United States | 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 |
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.