510(k) Report

FDA applicant

Strohl Medical Technologies

Kittery, ME1 decision2013–20130 recalls

FDA records 1 decision for Strohl Medical Technologies (Kittery, ME) in 2013: 1 510(k) clearance. All are in product code GWF (Stimulator, Electrical, Evoked Response). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Strohl Medical Technologies’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2013: 1
2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Strohl Medical Technologies by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GWFStimulator, Electrical, Evoked Response1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 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.

  • K123843Neuroepg SystemStrohl Medical Technologies · 20132cite it

What has FDA decided for it lately?

  • K123843Neuroepg SystemStrohl Medical Technologies · 2013

The one decision as Strohl Medical Technologies →