The Magstim Company Limited
The Magstim Company Limited holds FDA 510(k) medical device clearances, first cleared 2024, most recent 2025, with 6 FDA device recalls on record.
Top product codes for The Magstim Company Limited
FDA recalls by The Magstim Company Limited
- Z-0869-2021 — Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: indicated for use in stimulating and monitoring cranial motor nerves, especially the facial nerve (VII), during ENT surgical procedures.
- Z-2884-2020 — Neurosign V4 Intraoperative Nerve monitor family of devices.
- Z-1965-2020 — Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
- Z-1966-2020 — Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
- Z-0836-2019 — HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
- Z-1352-2018 — Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air Film Coil and Main Filters Product Usage For the treatment of major depressive disorders in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by The Magstim Company Limited
Data sourced from openFDA. This site is unofficial and independent of the FDA.