FDA applicant

Medical Action Industries, Inc.

Arden, NC8 decisions1981–20050 recalls

FDA records 8 decisions for Medical Action Industries, Inc. (Arden, NC) from 1981 to 2005: 8 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and NAB (Gauze / Sponge,Nonresorbable For External Use). Its devices cite 1 predicate, 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Medical Action Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Medical Action Industries, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?