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Sign in to claim this brandNeurovision Medical Product, Inc.
United States·US-MF-000029865
Last updated May 23, 2026
Information
- Country
- United States
- Address
- 4837, McGrath Steet, Ventura, United States
- Website
- neurovisionmedical.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Christine Vergely
- EUDAMED SRN
- US-MF-000029865
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (102)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nerveana+® | N/A | FDA UDI | Class II | Active |
| Scorpion | N/A | FDA UDI | Class II | Active |
| Dragonfly® | N/A | FDA UDI | Class II | Active |
| Dragonfly® | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Nerveana | N/A | FDA UDI | Class II | Active |
| Nerveäna+® | NONE | FDA UDI | Class II | Active |
| Scorpion | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Nerveana+® | N/A | FDA UDI | Class II | Active |
| Nerveäna+® | NONE | FDA UDI | Class II | Active |
| Nerveäna+® | NONE | FDA UDI | Class II | Active |
| Nerveana | N/A | FDA UDI | Class II | Active |
| Dragonfly® | N/A | FDA UDI | Class II | Active |
| Nerveana+® | N/A | FDA UDI | Class II | Active |
| Nerveana | N/A | FDA UDI | Class II | Active |
| Cobra® | N/A | FDA UDI | Class II | Active |
| Nerveana | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Cobra | N/A | FDA UDI | Class II | Active |
| Cobra® | N/A | FDA UDI | Class II | Active |
| Nerveana | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Dragonfly® | N/A | FDA UDI | Class II | Active |
| Dragonfly® | N/A | FDA UDI | Class II | Active |
| Nerveana+® | N/A | FDA UDI | Class II | Active |
| Nerveana+® | N/A | FDA UDI | Class II | Active |
| Dragonfly® | N/A | FDA UDI | Class II | Active |
| Dragonfly® | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Nerveana | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Dragonfly® | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Nerveana+® | N/A | FDA UDI | Class II | Active |
| Nerveana | N/A | FDA UDI | Class II | Unknown |
| Nerveäna+® | NONE | FDA UDI | Class II | Active |
| Nerveana+® | N/A | FDA UDI | Class II | Active |
| Nerveana+® | N/A | FDA UDI | Class II | Active |
| Dragonfly® | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Cobra | N/A | FDA UDI | Class II | Active |
| Scorpion | N/A | FDA UDI | Class II | Active |
| Nerveana | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Nerveana+® | N/A | FDA UDI | Class II | Active |
| Nerveana® | NONE | FDA UDI | Class II | Active |
| Nerveana | N/A | FDA UDI | Class II | Active |
| Nerveana+® | N/A | FDA UDI | Class II | Active |
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FDA Recalls (12)
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 |
|---|---|---|---|---|
| May 19, 2025 | Z-2100-2025 | — | open, classified | Product packaging contains the wrong part number and kit contents. |
| Jul 1, 2024 | Z-2719-2024 | — | open, classified | mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size. |
| Jul 21, 2020 | Z-2903-2020 | — | terminated | The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable. |
| Jul 21, 2020 | Z-2902-2020 | — | terminated | The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable. |
| Jul 21, 2020 | Z-2905-2020 | — | terminated | The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable. |
| Jul 21, 2020 | Z-2906-2020 | — | terminated | The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable. |
| Jul 21, 2020 | Z-2904-2020 | — | terminated | The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable. |
| Jul 21, 2020 | Z-2901-2020 | — | terminated | The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable. |
| Jul 21, 2020 | Z-2908-2020 | — | terminated | The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable. |
| Jul 21, 2020 | Z-2907-2020 | — | terminated | The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable. |
| Jul 21, 2020 | Z-2900-2020 | — | terminated | The electrode insulating material on the Cobra EMG ET tube used for continuous EMG monitoring may soften over time so that it may be more susceptible to damage by scratching or bending, which could stop or inhibit the EMG signal transmission of the electrodes to the monitor and render the device not usable. |
| Jan 11, 2010 | Z-0798-2010 | — | terminated | This recall has been initiated due to a conductive glue used to attach the lead wire to electrode, which has been found in a small number of electrodes, to cause a short circuit in one of the channels. This is due to migration of the adhesive from one pad to the other creating an electrical short. Use of one of these defective electrodes could lead to a failure to monitor. Our investigation has c |