Data / Medical devices / Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat / United States
FDA-registered makers of Ultrasonic Diathermy 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 Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat (product code IMI). 6 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
- Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat
- Product code
- IMI
- Country
- United States
Makers of Ultrasonic Diathermy 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 |
|---|---|---|---|---|---|---|---|---|
| Djo, LLC | Carlsbad, CA, United States | Specification developer | 2 | December 3, 2003 | 0 | 0 | 0 | api.fda.gov |
| Imex, LLC | Fulton, MD, United States | Manufacturer | 2 | October 22, 2003 | 0 | 0 | 0 | api.fda.gov |
| Kmi Imi Group / Dba: Innovative Med, Inc. | Irvine, CA, United States | Specification developer | 1 | August 9, 2001 | 0 | 0 | 0 | api.fda.gov |
| Manamed LLC | Denton, TX, United States | Specification developer | 1 | March 8, 2023 | 0 | 0 | 0 | api.fda.gov |
| Mettler Electronics Corp. | Anaheim, CA, United States | Manufacturer | 1 | May 4, 2006 | 0 | 0 | 0 | api.fda.gov |
| Preferred Depot | Irvine, CA, United States | Remanufacturer, Repackager or relabeler | 1 | August 25, 2017 | 0 | 0 | 0 | api.fda.gov |
| Amrex-Zetron, Inc. | Paramount, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ascentron, Inc. | White City, OR, 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.