FDA applicant

Euromed, Inc.

North Attleboro, MA4 decisions1998–20080 recalls

FDA records 4 decisions for Euromed, Inc. (North Attleboro, MA) from 1998 to 2008: 4 510(k) clearances. All are in product code FRO (Dressing, Wound, Drug). Its devices cite 14 predicates, 3 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

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

FDA decisions per year

1in 2008

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Euromed, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Euromed”

FDA records each applicant name separately; these may or may not be the same firm.

Euromed A/S 4

Euromed, 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?

Other applicant names beginning “Euromed”