FDA applicant

Artventive Medical Group, Inc.

Carlsbad, CA3 decisions2014–20220 recalls

FDA records 3 decisions for Artventive Medical Group, Inc. (Carlsbad, CA) from 2014 to 2022: 3 510(k) clearances. All are in product code KRD (Device, Vascular, For Promoting Embolization). Its devices cite 5 predicates, 2 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 Artventive Medical Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2014high 1 (2014) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Artventive Medical Group, Inc. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Artventive Medical Group, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?