Is this your brand? Sign in to claim ownership.
Sign in to claim this brandMYOTRONICS-NOROMED, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 5870 S. 194TH ST., KENT, WA, 98032
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3014732
- DUNS Number
- —
Catalogue (26)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| BNS-40 Home Treatment Unit | BNS-40 | FDA UDI | Class II | Active |
| Myotronics 6145 Duotrodes | 6145 | FDA UDI | Class II | Active |
| Norotrode 20 | N120 | FDA UDI | Class II | Active |
| K7 EMG Electromyograph | EMG | FDA UDI | Class II | Active |
| Myotrode One without Gel | 4070 | FDA UDI | Class II | Active |
| K7 Evaluation System-ESG | K7/ESG | FDA UDI | Class II | Active |
| Myotrode SG Solid Gel TENS Electrodes | 4300 | FDA UDI | Class II | Active |
| MES 9000 Dynamic EMG | MES 9000 EMG | FDA UDI | Class II | Active |
| K7 Evaluation System-CMS | K7/CMS | FDA UDI | Class I | Active |
| MES 9000 Musculoskeletal System | N9000M | FDA UDI | Class II | Active |
| MES 9000 Muscle Tester | Muscle Tester | FDA UDI | Class II | Active |
| Myotrode One With Gel | 4060 | FDA UDI | Class II | Active |
| J5 Myo-Monitor | J5 | FDA UDI | Class II | Active |
| K7 Evaluation System-EMG | K7/EMG | FDA UDI | Class II | Active |
| K7 CMS Sensor Array | K7 CMS Sensor Array | FDA UDI | Class I | Active |
| Noromed NT-360 Inclinometer | NT360 | FDA UDI | Class I | Active |
| K7 ESG-2 Electrosonograph | ESG-2 | FDA UDI | Class I | Active |
| MES 9000 Static Electromyography Scanner | Static EMG Scanner | FDA UDI | Class II | Active |
| Monotrode 101 | 101 | FDA UDI | Class II | Active |
| Myo-Trode Sg Disposable Electrode | K040400 | FDA 510(k) | Class II | Active |
| Emg System | K111687 | FDA 510(k) | Class II | Active |
| Norodyn 8000 Semg System, Nd-8000 | K992439 | FDA 510(k) | Class II | Active |
| Model K7 Evaluation Device | K003287 | FDA 510(k) | Class II | Active |
| Model Mes-9000/Emg System | K013399 | FDA 510(k) | Class II | Active |
| Modification To K6-I Diagnostic System, Model K6-I | K992694 | FDA 510(k) | Class II | Active |
| Model J-5 Mvo-Monitor | K031998 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.