Medical Device Manufacturer · GB , Whitland

Magstim Company, Ltd. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2017
10
Total
10
Cleared
0
Denied

Magstim Company, Ltd. has 10 FDA 510(k) cleared neurology devices. Based in Whitland, GB.

Latest FDA clearance: Mar 2023. Active since 2017.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

10 devices
1–10 of 10
Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+
K223154 · OBP Transcranial Magnetic Stimulator · Neurology
Mar 2023 161d
Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+
K222171 · OBP Transcranial Magnetic Stimulator · Neurology
Jan 2023 176d
Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, Horizon 3.0 with Navigation
K211389 · OBP Transcranial Magnetic Stimulator · Neurology
Sep 2021 132d
Neurosign V4 Intraoperative Nerve Monitor
K203684 · PDQ Neurosurgical Nerve Locator · Neurology
Mar 2021 90d
HORIZON TMS Therapy System with Navigation
K183376 · OBP Transcranial Magnetic Stimulator · Neurology
Apr 2019 118d
HORIZON TMS Therapy System
K182853 · OBP Transcranial Magnetic Stimulator · Neurology
Mar 2019 156d
Neurosign V4 Intraoperative Nerve Monitor
K181559 · PDQ Neurosurgical Nerve Locator · Neurology
Nov 2018 149d
HORIZON TMS Therapy System
K180907 · OBP Transcranial Magnetic Stimulator · Neurology
Aug 2018 119d
HORIZON Therapy System
K171051 · OBP Transcranial Magnetic Stimulator · Neurology
Sep 2017 156d
Rapid2 Therapy System
K162935 · OBP Transcranial Magnetic Stimulator · Neurology
Mar 2017 141d
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