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Data / Medical devices / Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat / United States

FDA-registered makers of Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat in the United States: 5 establishments

5 establishments in the United States are registered with the FDA to make Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat (product code ILX). 4 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
Product code
ILX
Country
United States

Makers of Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Endonovo TherapeuticsWoodland Hills, CA, United StatesSpecification developer2July 27, 2012000api.fda.gov
Orthocor Medical Inc.Blaine, MN, United StatesManufacturer2December 18, 2024000api.fda.gov
Bioelectronics CorporationJefferson, MD, United StatesComplaint file establishment, Manufacturer, Specification developer1June 28, 2019000api.fda.gov
Regenesis Biomedical, Inc.Scottsdale, AZ, United StatesSpecification developer1December 13, 2013010api.fda.gov
Adm Tronics Unltd, Inc.Northvale, NJ, United StatesContract manufacturer0000api.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.