510(k) Report

FDA applicant

Artiria Medical SA

Geneva, CH1 decision2023–20230 recalls

FDA records 1 decision for Artiria Medical SA (Geneva, CH) in 2023: 1 510(k) clearance. All are in product code MOF (Guide, Wire, Catheter, Neurovasculature). Its devices cite 2 predicates, 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, cardiovascular panel, where it files most

How often FDA has decided Artiria Medical SA’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2023: 1
2023high 1 (2023) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2023.

FIG. 1 — Artiria Medical SA by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MOFGuide, Wire, Catheter, Neurovasculature1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K222690SmartGUIDE deflectable hydrophilic guidewireArtiria Medical SA · 2023

The one decision as Artiria Medical SA →