# Neurosteer, Inc.

- Location (FDA's records): New York, NY
- FDA decisions: 1 (2022–2022): 1 510(k) clearance
- Product codes: OMC (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ceribell, Inc.: 2 (https://510kreport.com/company/ceribell)

## Firms that cite its devices most
- NeuroServo, Inc.: 1 (https://510kreport.com/company/neuroservo)
- Qx World, Ltd.: 1 (https://510kreport.com/company/qx-world)

## Its most-cited devices
- K221563: Neurosteer EEG Recorder (2022), cited by 2

## Recent decisions
- K221563: Neurosteer EEG Recorder (Oct 24, 2022)

Source page: https://510kreport.com/company/neurosteer