Data / Medical devices / Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat / United States
FDA-registered makers of Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat (product code IMJ). 5 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
- Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat
- Product code
- IMJ
- Country
- United States
Makers of Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Accelerated Care Plus Corp. | Reno, NV, United States | Repackager or relabeler, Specification developer | 1 | June 14, 2016 | 0 | 0 | 0 | api.fda.gov |
| Djo, LLC | Carlsbad, CA, United States | Specification developer | 1 | March 18, 2009 | 0 | 0 | 0 | api.fda.gov |
| Mettler Electronics Corp. | Anaheim, CA, United States | Manufacturer | 1 | October 8, 2004 | 0 | 0 | 0 | api.fda.gov |
| Promedtek, Inc. | Scottsdale, AZ, United States | Repackager or relabeler, Specification developer | 1 | November 17, 2016 | 0 | 0 | 0 | api.fda.gov |
| Regenesis Biomedical, Inc. | Scottsdale, AZ, United States | Specification developer | 1 | May 24, 2023 | 0 | 0 | 0 | api.fda.gov |
| Amrex-Zetron, Inc. | Paramount, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hda Technology, Inc. | Lake Forest, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Velentium Medical | Richmond, TX, 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.