Data / Medical devices / United States / Motive Health, Inc.
Motive Health, Inc.: FDA-registered device maker in Tempe, AZ, United States, 5 510(k) clearances
Motive Health, Inc. is registered with the FDA (registration 3011466827) in Tempe, AZ, United States. It lists 7 device types. The FDA files 5 510(k) clearances under its listings, the newest dated November 6, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011466827
- Address
- 2120 East 6th Street Suite 8, Tempe, AZ, United States, 85288
- Owner or operator
- Motive Health, Inc. (10049027)
- Roles
- Manufacturer, Specification developer
- First device listed
- April 3, 2015
- Registered through
- 2026
- Brand names listed
- CyMedica e-vive System; CY-1000, IntellihabSystem, Motive Knee Wrap, Motive Muscle Stimulator for Lower Back, Motive Electrode, QB1 Powered Muscle Stimulator System (NMES) & Transcutaneous Electrical Nerve Stimulator System (TENS); QB-1000
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Cutaneous | GXY | 2 | Manufacturer | accessdata.fda.gov |
| Goniometer, Ac-Powered | KQX | 1 | Manufacturer | accessdata.fda.gov |
| Joint, Knee, External Brace | ITQ | 1 | Manufacturer | accessdata.fda.gov |
| Medical Device Data System | OUG | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 6, 2025 | K253478 | Motive Muscle Stimulator for Lower Back (OT01-1003) | NGX | Substantially Equivalent | Motive Health, Inc. | accessdata.fda.gov |
| March 22, 2023 | K230533 | Motive Electrode | GXY | Substantially Equivalent | Cymedica Orthopedics, Inc. | accessdata.fda.gov |
| May 12, 2022 | K220738 | Motive Knee Wrap | IPF | Substantially Equivalent | Cymedica Orthopedics, Inc. | accessdata.fda.gov |
| December 1, 2016 | K163067 | CyMedica e-vive System; CY-1000 | IPF | Substantially Equivalent | Cymedica Orthopedics, Inc. | accessdata.fda.gov |
| April 2, 2015 | K150413 | QB1 System Powered Muscle Stimulator & Transcutaneous Electrical Nerve Stimulator | IPF | Substantially Equivalent | Cymedica Orthopedics, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Medical Device Data System
- All makers of Stimulator, Muscle, Powered
- All makers of Electrode, Cutaneous
- All makers of Joint, Knee, External Brace
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Goniometer, Ac-Powered
Updated November 6, 2025. 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.