# Neurent Medical

- Location (FDA's records): Galway, IE
- FDA decisions: 4 (2021–2026): 4 510(k) clearances
- Names in FDA's records: Neurent Medical (2); Neurent Medical , Ltd. (2)
- Product codes: GEI (4)
- 510(k) review time since 2016: median 84 days, against 148 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 4 (3 its own); citations of its devices by later devices: 3 (3 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
- Aerin Medical, Inc.: 1 (https://510kreport.com/company/aerin-medical)

## Its most-cited devices
- K222032: NEUROMARK System (2022), cited by 1
- K250048: NEUROMARK System (NMK00301) (2025), cited by 1
- K212666: Neuromark System (2021), cited by 1

## Recent decisions
- K261833: NEUROMARK System (NMK00301) (Jun 16, 2026)
- K250048: NEUROMARK System (NMK00301) (May 29, 2025)
- K222032: NEUROMARK System (Oct 26, 2022)
- K212666: Neuromark System (Oct 22, 2021)

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