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Data / Medical devices / Interferential Current Therapy / United States

FDA-registered makers of Interferential Current Therapy in the United States: 19 establishments

19 establishments in the United States are registered with the FDA to make Interferential Current Therapy (product code LIH). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

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Device
Interferential Current Therapy
Product code
LIH
Country
United States

Makers of Interferential Current Therapy in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Biowave CorporationNorwalk, CT, United StatesManufacturer, Specification developer1December 13, 2005000api.fda.gov
BioMedical Life Systems Inc.Carlsbad, CA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer1April 29, 2004000api.fda.gov
Rst-SanexasHenderson, NV, United StatesManufacturer1January 24, 2003000api.fda.gov
Surgitech, Inc.Carlsbad, CA, United StatesSpecification developer1November 14, 2003000api.fda.gov
VQ OrthocareVista, CA, United StatesManufacturer1June 12, 2019000api.fda.gov
Ascentron, Inc.White City, OR, United StatesContract manufacturer0000api.fda.gov
Altivera Medical, Inc.Englewood, CO, United StatesManufacturer0000api.fda.gov
Clearlake-Tech IncClear Lake, SD, United StatesContract manufacturer0000api.fda.gov
Distron CorporationAttleboro Falls, MA, United StatesContract manufacturer0000api.fda.gov
Djo, LLCCarlsbad, CA, United StatesManufacturer, Specification developer0000api.fda.gov
Drive Northpoint, LLCPalmetto, GA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Electrostim Medical Services, Inc.Tampa, FL, United StatesSpecification developer0000api.fda.gov
Imex, LLCFulton, MD, United StatesManufacturer0000api.fda.gov
Jomel Seams Reasonable LLCHillside, NJ, United StatesContract manufacturer0000api.fda.gov
Liberty Medical Solutions, LLCTampa, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Mettler Electronics Corp.Anaheim, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Neurological Fitness Equipment And Education LLCAustin, TX, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Preferred DepotIrvine, CA, United StatesRemanufacturer, Repackager or relabeler0000api.fda.gov
RS MedicalVancouver, WA, United StatesManufacturer0000api.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.