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Sign in to claim this brandMOTION CONTROL, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 115 N WRIGHT BROTHERS DR, SALT LAKE CITY, UT, 84116
- Website
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3001237006
- DUNS Number
- —
Catalogue (5)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Myolab Ii | MC-200 | FDA UDI | Class II | Active |
| Dermatron Iontophoresis Device | K780310 | FDA 510(k) | N/A | Active |
| Phoresor Ii (tm), Model Pm700 | K872040 | FDA 510(k) | Class II | Active |
| Myolab Ii, Model Ml-200 | K862236 | FDA 510(k) | Class II | Active |
| Utah Artifical Arm | K802642 | FDA 510(k) | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
Not available yet.
Authorities
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Feb 1, 2005 | Z-0959-05 | — | terminated | Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard. |