Data / Medical devices / Massager, Powered Inflatable Tube / United States
FDA-registered makers of Massager, Powered Inflatable Tube in the United States: 28 establishments
28 establishments in the United States are registered with the FDA to make Massager, Powered Inflatable Tube (product code IRP). 22 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
- Massager, Powered Inflatable Tube
- Product code
- IRP
- Country
- United States
Makers of Massager, Powered Inflatable Tube in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Normatec Industries, LP | Watertown, MA, United States | Specification developer | 8 | October 6, 2026 | 0 | 0 | 0 | api.fda.gov |
| Joicom Corporation | Eastvale, CA, United States | Complaint file establishment, Manufacturer, Specification developer | 7 | November 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| Zenith Technical Innovations, LLC | Gurnee, IL, United States | Manufacturer | 4 | July 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| Avanos Medical, Inc. | Alpharetta, GA, United States | Complaint file establishment, Specification developer | 3 | January 31, 2025 | 0 | 0 | 0 | api.fda.gov |
| Rapid Reboot Recovery Products | Lindon, UT, United States | Manufacturer, Remanufacturer, Repackager or relabeler | 3 | December 22, 2020 | 0 | 0 | 0 | api.fda.gov |
| Bio Compression Systems, Inc. | Moonachie, NJ, United States | Manufacturer | 2 | February 16, 2022 | 0 | 0 | 0 | api.fda.gov |
| Mueller Sports Medicine, Inc. | Prairie Du Sac, WI, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 2 | May 15, 2019 | 0 | 0 | 0 | api.fda.gov |
| Portable Therapeutix | Houston, TX, United States | Repackager or relabeler, Specification developer | 2 | March 11, 2014 | 0 | 0 | 0 | api.fda.gov |
| Therabody, Inc. | Los Angeles, CA, United States | Complaint file establishment, Specification developer | 2 | August 30, 2024 | 0 | 0 | 0 | api.fda.gov |
| VIVE Health LLC | Naples, FL, United States | Repackager or relabeler, Specification developer | 2 | August 2, 2024 | 0 | 0 | 0 | api.fda.gov |
| Aquilo Sports L.L.C. | Louisville, KY, United States | Repackager or relabeler, Specification developer | 1 | November 4, 2022 | 0 | 0 | 0 | api.fda.gov |
| B.I.G. Logistics LLC | Dallas, TX, United States | Complaint file establishment, Specification developer | 1 | February 22, 2021 | 0 | 0 | 0 | api.fda.gov |
| Breg, Inc. | Carlsbad, CA, United States | Specification developer | 1 | March 1, 2019 | 0 | 0 | 0 | api.fda.gov |
| Compression Solutions, LLC | Charlotte, NC, United States | Specification developer | 1 | November 21, 2012 | 0 | 0 | 0 | api.fda.gov |
| Eva Medtec, Inc | Shakopee, MN, United States | Manufacturer | 1 | March 5, 2021 | 0 | 0 | 0 | api.fda.gov |
| Fist Assist Devices, LLC | Las Vegas, NV, United States | Specification developer | 1 | June 17, 2021 | 0 | 0 | 0 | api.fda.gov |
| Hanuri Distribution, Inc | Chatsworth, CA, United States | Manufacturer | 1 | October 21, 2020 | 0 | 0 | 0 | api.fda.gov |
| Manamed LLC | Denton, TX, United States | Specification developer | 1 | August 5, 2020 | 0 | 0 | 0 | api.fda.gov |
| Medical Quant Usa | Solon, OH, United States | Specification developer | 1 | June 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| Menlo Brands | Menlo Park, CA, United States | Specification developer | 1 | September 19, 2019 | 0 | 0 | 0 | api.fda.gov |
| Merchsource LLC | Irvine, CA, United States | Specification developer | 1 | October 30, 2025 | 0 | 0 | 0 | api.fda.gov |
| Nice Recovery Systems LLC | Boulder, CO, United States | Manufacturer | 1 | December 23, 2014 | 0 | 0 | 0 | api.fda.gov |
| Albert International, Inc. | Gainesville, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| All Quality & Services, Inc. | Fremont, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| All Quality & Services, Inc. | Garland, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gregory MFG., Inc. | Holyoke, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ivy Technology | Jeffersontown, KY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PRIDE Industries | Roseville, CA, 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.