Home › Device types › NHI
Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief
FDA product code NHI · Class 2 · Neurology
125
Registered devices
75
Adverse events
0
Recalls
13
510(k) clearances
Devices with this code
SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.BiowavePRO — BIOWAVE CORPORATIONSPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT™ — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT™ — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT — SPR THERAPEUTICS, INC.SPRINT™ — SPR THERAPEUTICS, INC.
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
