FDA applicant

Therasigma, LLC

Washougal, WA2 decisions2020–20210 recalls

FDA records 2 decisions for Therasigma, LLC (Washougal, WA) from 2020 to 2021: 2 510(k) clearances. Most are in product codes LIH (Interferential Current Therapy) and IPF (Stimulator, Muscle, Powered). 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 Therasigma, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2020high 1 (2020) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Therasigma, LLC by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Therasigma, LLC

Which product codes does it file in?

What has FDA decided for it lately?