Data / Medical devices / Stimulator, Muscle, Powered / United States
FDA-registered makers of Stimulator, Muscle, Powered in the United States: 43 establishments
43 establishments in the United States are registered with the FDA to make Stimulator, Muscle, Powered (product code IPF). 21 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.
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- Device
- Stimulator, Muscle, Powered
- Product code
- IPF
- Country
- United States
Makers of Stimulator, Muscle, Powered 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 | Manufacturer, Specification developer | 13 | April 14, 2016 | 0 | 0 | 0 | api.fda.gov |
| Mettler Electronics Corp. | Anaheim, CA, United States | Manufacturer, Repackager or relabeler | 4 | March 21, 2024 | 0 | 0 | 0 | api.fda.gov |
| Altivera Medical, Inc. | Englewood, CO, United States | Manufacturer | 3 | January 26, 2024 | 0 | 0 | 0 | api.fda.gov |
| BioMedical Life Systems Inc. | Carlsbad, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 3 | August 19, 2003 | 0 | 0 | 0 | api.fda.gov |
| Drive Northpoint, LLC | Palmetto, GA, United States | Manufacturer, Repackager or relabeler | 3 | October 2, 2017 | 0 | 0 | 0 | api.fda.gov |
| Motive Health, Inc. | Tempe, AZ, United States | Manufacturer | 3 | May 12, 2022 | 0 | 0 | 0 | api.fda.gov |
| Electronic Waveform Lab, Inc. | Huntingtn Bch, CA, United States | Manufacturer, Specification developer | 2 | June 1, 2011 | 0 | 0 | 0 | api.fda.gov |
| Electrostim Medical Services, Inc. | Tampa, FL, United States | Specification developer | 2 | October 21, 2022 | 0 | 0 | 0 | api.fda.gov |
| Accelerated Care Plus Corp. | Reno, NV, United States | Remanufacturer, Repackager or relabeler, Specification developer | 1 | May 2, 1995 | 0 | 0 | 0 | api.fda.gov |
| Ampcare, LLC | Fort Worth, TX, United States | Manufacturer | 1 | October 31, 2013 | 0 | 0 | 0 | api.fda.gov |
| Dynapulse Medical LLC | Minnetonka, MN, United States | Specification developer | 1 | January 30, 2008 | 0 | 0 | 0 | api.fda.gov |
| Elite Medical Supply Of New York, LLC | Hendersonville, TN, United States | Manufacturer, Specification developer | 1 | November 18, 2004 | 0 | 0 | 0 | api.fda.gov |
| Integrated Biomedical Corp. | Las Vegas, NV, United States | Manufacturer | 1 | December 14, 1984 | 0 | 0 | 0 | api.fda.gov |
| Liberty Medical Solutions, LLC | Tampa, FL, United States | Manufacturer, Repackager or relabeler | 1 | February 12, 2010 | 0 | 1 | 0 | api.fda.gov |
| Med Labs, Inc. | Goleta, CA, United States | Manufacturer | 1 | September 6, 1996 | 0 | 0 | 0 | api.fda.gov |
| Prizm Medical, Inc. | Buford, GA, United States | Contract manufacturer, Contract sterilizer, Manufacturer, Repackager or relabeler, Specification developer | 1 | November 21, 1995 | 0 | 0 | 0 | api.fda.gov |
| REACT Innovations | Charlotte, NC, United States | Manufacturer | 1 | May 21, 1998 | 0 | 0 | 0 | api.fda.gov |
| Restorative Therapies Inc. | Nottingham, MD, United States | Manufacturer | 1 | December 16, 2016 | 0 | 0 | 0 | api.fda.gov |
| RS Medical | Vancouver, WA, United States | Manufacturer | 1 | January 19, 2012 | 0 | 1 | 0 | api.fda.gov |
| Therabody, Inc. | Los Angeles, CA, United States | Complaint file establishment, Specification developer | 1 | July 30, 2021 | 0 | 0 | 0 | api.fda.gov |
| VQ Orthocare | Vista, CA, United States | Manufacturer | 1 | November 16, 2020 | 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 | |
| Bioness Medical, Inc. | Valencia, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioventus LLC | Cordova, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CIONIC Facility | Scotts Valley, CA, United States | Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Clear Blue Engineering, Inc. | Lafayette, CO, United States | Contract 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 | |
| Draeger Medical Systems, Inc. | Andover, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Imex, LLC | Fulton, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Katecho LLC | Des Moines, IA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| KL Distributing | Hudson, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Manamed LLC | Denton, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neuralace Medical | San Marcos, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neuro20 Technologies Corp. | Oldsmar, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neurological Fitness Equipment And Education LLC | Austin, TX, United States | Complaint file establishment, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neuvotion, Inc. | Stamford, CT, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pemf Systems, Inc. | Las Vegas, NV, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Preferred Depot | Irvine, CA, United States | Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Raja Trading Company, Inc. | Fairfax, VA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rst-Sanexas | Henderson, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Synapse Biomedical Inc. | Oberlin, OH, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Theragen, Inc. | Jacksonville, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.