Magstim Company Limited - FDA 510(k) Cleared Devices

Magstim Company Limited, is a neurotechnology company specializing in brain stimulation and neurophysiological monitoring solutions. Based in Carmarthenshire, UK, the company develops electroencephalography (EEG), transcranial magnetic stimulation (TMS), and transcranial direct current stimulation (tDCS) technologies for researchers and clinicians worldwide.

The company received 1 FDA 510(k) clearance from 1 total submission, with its cleared device in the Neurology category. The clearance was granted in 2015. Magstim has not received additional FDA 510(k) clearances since that time and should be treated as a historical regulatory record.

Magstim's product portfolio includes research and clinical TMS systems, HD-EEG solutions, and portable tDCS devices. The company operates across more than 115 regions globally and maintains a strong presence in neuroscience research, with over 20,000 clinical citations supporting its technologies. The brand is recognized as a pioneer in TMS innovation with more than 30 years of industry experience.

For detailed information on cleared device names, product codes, and clearance dates, explore the full 510(k) database record.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.