# Neurovision Medical Products, Inc.

- Location (FDA's records): Ventura, CA
- FDA decisions: 9 (2010–2013): 9 510(k) clearances
- Product codes: ETN (5), BZQ (1), PDQ (1), GWF (1), FAP (1)
- Predicates its devices cite: 14 (2 its own); citations of its devices by later devices: 6 (2 its own)
- Recalls linked to its devices: 12 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Rln Systems, Inc.: 5 (https://510kreport.com/company/rln-systems)
- Nuvasive, Inc.: 2 (https://510kreport.com/company/nuvasive)
- Gereonics, Inc.: 1 (https://510kreport.com/company/gereonics)
- R & D Medical Products, Inc.: 1 (https://510kreport.com/company/r-d-medical-products)
- 3M Company: 1 (https://510kreport.com/company/3m)
- Axon Systems, Inc.: 1 (https://510kreport.com/company/axon-systems)
- Dantec Electronics, Inc.: 1 (https://510kreport.com/company/dantec-electronics)

## Firms that cite its devices most
- Inomed Medizintechnik GmbH: 2 (https://510kreport.com/company/inomed-medizintechnik)
- Spes Medica Srl: 1 (https://510kreport.com/company/spes-medica)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)

## Its most-cited devices
- K110989: Neurovision Ink Printed Endotracheal Tube Electrode (2011), cited by 3
- K110712: Drytouch Suction Stimulator Probe (2011), cited by 2
- K110140: Neurovision Nerve Locator Monitor (2011), cited by 1

## Recent decisions
- K130570: Neurovision Medical Motion Sensor (Dec 26, 2013)
- K130806: Neurovision Ink Printed Endotracheal Tube Electrode (Jul 12, 2013)
- K113771: Signal Gear Urethral Catheter Electrode (Dec 13, 2012)
- K121931: Nondisposable Stimulating Instruments (Oct 19, 2012)
- K110989: Neurovision Ink Printed Endotracheal Tube Electrode (Nov 3, 2011)
- K110140: Neurovision Nerve Locator Monitor (Sep 30, 2011)
- K110712: Drytouch Suction Stimulator Probe (Jun 28, 2011)
- K110138: Paired Hydrogel Electrode (Apr 8, 2011)

Source page: https://510kreport.com/company/neurovision-medical-products