510(k) Report

FDA applicant

Chirurgie Innovation

Massy, FR2 decisions2017–20220 recalls

FDA records 2 decisions for Chirurgie Innovation (Massy, FR) from 2017 to 2022: 2 510(k) clearances. All are in product code FAS (Electrode, Electrosurgical, Active, Urological). Its devices cite 3 predicates, 1 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 Chirurgie Innovation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2017: 12022: 1
2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Chirurgie Innovation by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • FASElectrode, Electrosurgical, Active, Urological2decisions

Whose devices does it build on?

Its devices cite 3 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 times; 1 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.

  • K163090Plasma Edge SystemChirurgie Innovation · 20171cites it
  • K213135Plasma Edge resection and vaporization electrodes, Plasma Edge working elements, Adaptor Plasma EdgeChirurgie Innovation · 20221cites it

What has FDA decided for it lately?

  • K213135Plasma Edge resection and vaporization electrodes, Plasma Edge working elements, Adaptor Plasma EdgeChirurgie Innovation · 2022
  • K163090Plasma Edge SystemChirurgie Innovation · 2017

All 2 as Chirurgie Innovation →