Medical Device Manufacturer · US , Malvern , PA

Neuronetics, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2016
8
Total
8
Cleared
0
Denied

Neuronetics, Inc. has 8 FDA 510(k) cleared medical devices. Based in Malvern, US.

Latest FDA clearance: Mar 2024. Active since 2016. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Neuronetics, Inc. Filter by specialty or product code using the sidebar.

8 devices
1–8 of 8
NeuroStar Advanced Therapy System (All previously cleared models)
K231926 · OBP Transcranial Magnetic Stimulator · Neurology
Mar 2024 266d
NeuroStar, NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar Advanced Therapy System for Mental Health
K222230 · OBP Transcranial Magnetic Stimulator · Neurology
Aug 2022 30d
NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar, NeuroStar Advanced Therapy for Mental Health
K220127 · OBP Transcranial Magnetic Stimulator · Neurology
Jul 2022 178d
NeuroStar Advanced Therapy for adjunctive treatment of OCD, NeuroStar Advanced Therapy System, NeuroStar TMS Therapy System, NeuroStar Advanced Therapy for Mental Health, NeuroStar
K212289 · QCI Transcranial Magnetic Stimulation System For Obsessive-compulsive Disorder · Neurology
May 2022 289d
NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar, NeuroStar Advanced Therapy for Mental Health
K213543 · OBP Transcranial Magnetic Stimulator · Neurology
Dec 2021 32d
NeuroStar Advanced Therapy
K201158 · OBP Transcranial Magnetic Stimulator · Neurology
Nov 2020 204d
NeuroStar TMS Therapy System
K161519 · OBP Transcranial Magnetic Stimulator · Neurology
Sep 2016 101d
NeuroStar TMS Therapy System
K160703 · OBP Transcranial Magnetic Stimulator · Neurology
Jun 2016 88d
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