510(k) Report

FDA applicant

Magstim Company Us, LLC

Woburn, MA1 decision2006–20060 recalls

FDA records 1 decision for Magstim Company Us, LLC (Woburn, MA) in 2006: 1 510(k) clearance. All are in product code GWF (Stimulator, Electrical, Evoked Response). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Magstim Company Us, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Magstim Company Us, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Magstim Company Us, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Magstim Company Us, LLC’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • GWFStimulator, Electrical, Evoked Response1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K060847Magstim 200-2Magstim Company Us, LLC · 20063cite it

What has FDA decided for it lately?

  • K060847Magstim 200-2Magstim Company Us, LLC · 2006

The one decision as Magstim Company Us, LLC →

Other applicant names beginning “Magstim”

FDA records each applicant name separately; these may or may not be the same firm.

The Magstim Company, Ltd. 27Magstim Corporation US 1