Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 7 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Magstim with 29 510(k) clearances and 6 device recalls. The most recent is a device recall dated Dec 8, 2020: Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: ind….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Dec 8, 2020 | Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: indicated for use in stimulating and monitoring cranialClass II · A small number of Neurosign 100 Intraoperative Nerve Monitors may have been dispatched without being configured appropri | Device recalls |
| Jun 23, 2020 | Neurosign V4 Intraoperative Nerve monitor family of devices.Class II · Reports that manipulation of the cable which connects the pre-amplifier to the nerve monitor, and the cable which connec | Device recalls |
| Mar 23, 2020 | Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive Disorder in adult patientClass II · It was identified that there is a potential for the Stim Interconnecting high Voltage Cable located at the rear of the R | Device recalls |
| Mar 23, 2020 | Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for the treatment of Major Depressive Disorder in adult patients who haveClass II · It was identified that there is a potential for the Stim Interconnecting high Voltage Cable located at the rear of the R | Device recalls |
| Oct 25, 2018 | HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)Class II · A stray strand of stainless-steel cable may protrude from the heat shrink sleeving on the Balance Cable of the Ez Arm. | Device recalls |
| Sep 28, 2017 | Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air Film Coil and Main FClass II · Users manuals not supplied with 4800-00T US Rapid Therapy System | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
