FDA applicant

Arteria Medical Science, Inc.

Newburyport, MA3 decisions2001–20020 recalls

FDA records 3 decisions for Arteria Medical Science, Inc. (Newburyport, MA) from 2001 to 2002: 3 510(k) clearances. Most are in product codes MJN (Catheter, Intravascular Occluding, Temporary) and FPB (Filter, Infusion Line). Its devices cite 3 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 Arteria Medical Science, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arteria Medical Science, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Arteria Medical Science, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Arteria Medical Science, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?