Data / Medical devices / Vibrator, Therapeutic / United States
FDA-registered makers of Vibrator, Therapeutic in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Vibrator, Therapeutic (product code IRO). 0 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
- Vibrator, Therapeutic
- Product code
- IRO
- Country
- United States
Makers of Vibrator, Therapeutic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aqp One, Inc. | Garden Grove, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Blaine Labs, Inc. | Santa Fe Springs, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Deep Muscle Stimulator, Inc. | Las Vegas, NV, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Djo, LLC | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inharmony Interactive | Las Vegas, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lotions Limited | Madison, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| North Coast Medical, Inc. | Morgan Hill, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Protocol Solutions LLC | Branson, MO, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rapid Release Technologies | Costa Mesa, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rezzimax, LLC | Smithfield, UT, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Pettibon System | Chehalis, WA, United States | Manufacturer | 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 | |
| Vibetech Enterprises, LLC | Sheboygan, WI, United States | 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.