# Neuspera Medical, Inc.

- Location (FDA's records): San Jose, CA
- FDA decisions: 3 (2021–2025): 2 510(k) clearances and 1 original PMA approval
- Product codes: GZF (2), EZW (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 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
- Boston Scientific Neuromodulation: 1 (https://510kreport.com/company/boston-scientific-neuromodulation)

## Its most-cited devices
- K202781: Neuspera Neurostimulation System (NNS) (2021), cited by 1

## Recent decisions
- P240031: Neuspera Sacral Neuromodulation System (Jun 17, 2025)
- K221303: Neuspera Nuity System (Apr 11, 2023)
- K202781: Neuspera Neurostimulation System (NNS) (Aug 27, 2021)

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