Magstim Company, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Magstim Company, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+, Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, H3.0, Horizon 3.0 with StimGuide+, Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0, Horizon 3.0 with Navigation
10
Total
10
Cleared
0
Denied
Magstim Company, Ltd. has 10 FDA 510(k) cleared neurology devices. Based in Whitland, GB.
Last cleared in 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.
FDA 510(k) Regulatory Record - Magstim Company, Ltd.
10 devices
Cleared
Mar 16, 2023
Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0,...
Neurology
161d
Cleared
Jan 13, 2023
Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0,...
Neurology
176d
Cleared
Sep 14, 2021
Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System, Horizon 3.0,...
Neurology
132d
Cleared
Mar 17, 2021
Neurosign V4 Intraoperative Nerve Monitor
Neurology
90d
Cleared
Apr 03, 2019
HORIZON TMS Therapy System with Navigation
Neurology
118d
Cleared
Mar 15, 2019
HORIZON TMS Therapy System
Neurology
156d
Cleared
Nov 09, 2018
Neurosign V4 Intraoperative Nerve Monitor
Neurology
149d
Cleared
Aug 03, 2018
HORIZON TMS Therapy System
Neurology
119d
Cleared
Sep 13, 2017
HORIZON Therapy System
Neurology
156d
Cleared
Mar 10, 2017
Rapid2 Therapy System
Neurology
141d