Data / Medical devices / Pad, Heating, Powered / United States
FDA-registered makers of Pad, Heating, Powered in the United States: 33 establishments
33 establishments in the United States are registered with the FDA to make Pad, Heating, Powered (product code IRT). 2 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
- Pad, Heating, Powered
- Product code
- IRT
- Country
- United States
Makers of Pad, Heating, Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Avacen, Inc. | Carlsbad, CA, United States | Manufacturer | 1 | August 15, 2014 | 0 | 0 | 0 | api.fda.gov |
| Richway & Fuji Bio Inc. | Honolulu, HI, United States | Complaint file establishment, Specification developer | 1 | February 8, 2008 | 0 | 0 | 0 | api.fda.gov |
| Amarigo Inc | Los Angeles, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Anodyne Therapy, LLC | Oldsmar, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Arlington Scientific, Inc. | Springville, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Babson Diagnostics | Austin, TX, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bear Down Brands, LLC | Fullerton, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Brace Align | Soddy Daisy, TN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Battle Creek Equipment | Fremont, IN, United States | Manufacturer, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| BlephEx, LLC | Brentwood, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cogmedix | West Boylston, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Conair LLC. | Stamford, CT, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Djo, LLC | Carlsbad, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Domico Med-Device, LLC | Fenton, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hyperice, Inc. | Irvine, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| KL Distributing | Hudson, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kaz USA, Inc., A Helen of Troy Company | Marlborough, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| King Brand Healthcare Products | Bellingham, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Merchsource LLC | Irvine, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Miller Technical Services | Plymouth, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Millstone Medical Outsourcing LLC | Olive Branch, MS, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Normatec Industries, LP | Watertown, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| OCuSOFT LLC | Rosenberg, TX, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orthocor Medical Inc. | Blaine, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| OcuSci Inc. | Del Mar, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pixie Cup LLC | Walnut Shade, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rechar Inc. | Strasburg, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Robotic Precision Therapy, LLC | Troy, MI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rog Sports Medicine, Inc. | Orland Park, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sharkninja Operating LLC | Needham, MA, United States | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sunbeam Products, Inc. | Atlanta, GA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Therabody, Inc. | Los Angeles, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| U.S. Surgitech, Inc. | Carol Stream, IL, United States | Repackager or relabeler, Specification developer | 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.