FDA applicant
Nevro Corporation
FDA records 1 decision for Nevro Corporation (Redwood City) in 2015: 1 original PMA approval. All are in product code LGW (Stimulator, Spinal-Cord, Totally Implanted For…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Nevro Corporation’s devices, and how often a recall has named them.
FDA decisions per year
1in 2015
2015high 1 (2015) · low 0 (2016)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2015.
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