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Stimulator, Electrical, Implanted, For Parkinsonian Symptoms
FDA product code NHL · Class 3 · Unknown
312
Registered devices
1,810
Adverse events
4
Recalls
0
510(k) clearances
Devices with this code
Vercise Genus™ — BOSTON SCIENTIFIC NEUROMODULATION CORPORATIONNA — MEDTRONIC, INC.NA — BOSTON SCIENTIFIC NEUROMODULATION CORPORATIONN/A — MEDTRONIC, INC.SenSight™ — MEDTRONIC, INC.N/A — MEDTRONIC, INC.Liberta RC™ — ADVANCED NEUROMODULATION SYSTEMS, INC.NA — BOSTON SCIENTIFIC NEUROMODULATION CORPORATIONNA — MEDTRONIC, INC.ACTIVA® Therapy — MEDTRONIC, INC.NA — MEDTRONIC, INC.DBS™ — MEDTRONIC, INC.N/A — MEDTRONIC, INC.Percept™ PC BrainSense™ — MEDTRONIC, INC.NA — MEDTRONIC, INC.Assess Review ™ — MEDTRONIC, INC.N/A — MEDTRONIC, INC.Vercise™ — BOSTON SCIENTIFIC NEUROMODULATION CORPORATIONNA — MEDTRONIC, INC.Vercise™ Cartesia™ X — BOSTON SCIENTIFIC NEUROMODULATION CORPORATIONNA — MEDTRONIC, INC.DBS™ — MEDTRONIC, INC.DBS™ — MEDTRONIC, INC.NA — ST. JUDE MEDICAL, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-07-08 | Boston Scientific Neuromodulation Corporation | Resistance and difficulties could occur while closing the retaining clip locking mechanism, which is part of a burr hole cover kit, which is part of a Deep Brai |
| 2025-07-08 | Boston Scientific Neuromodulation Corporation | Wire break(s) have occurred in rechargeable deep brain stimulation implantable pulse generators, implanted in the submuscular pectoral location. Wire breaks pre |
| 2024-04-18 | Boston Scientific Neuromodulation Corporation | Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may experience routine system check during IPG charging, which may cause device reset. The device |
| 2019-04-24 | Boston Scientific Neuromodulation Corporation | The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due t |
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