FDA applicant

Marwood Medical, Inc.

Greensboro, NC7 decisions1984–19850 recalls

FDA records 7 decisions for Marwood Medical, Inc. (Greensboro, NC) from 1984 to 1985: 7 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and DRE (Dilator, Vessel, For Percutaneous…). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Marwood Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Marwood Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?