510(k) Report

FDA applicant

Exodus Innovations

Sufa, IL1 decision2021–20210 recalls

FDA records 1 decision for Exodus Innovations (Sufa, IL) in 2021: 1 510(k) clearance. All are in product code NAM (Stimulator, Peripheral Nerve, Non-Implanted…). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Exodus Innovations’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021: 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Exodus Innovations by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • NAMStimulator, Peripheral Nerve, Non-Implanted, For Urinary Incontinence1decision

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 1 time; 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.

  • K192731ZIDA Wearable Neuromodulation SystemExodus Innovations · 20211cites it

What has FDA decided for it lately?

  • K192731ZIDA Wearable Neuromodulation SystemExodus Innovations · 2021

The one decision as Exodus Innovations →