FDA applicant

Flynt Amtex, Inc.

Burlington, NC1 decision1996–19960 recalls

FDA records 1 decision for Flynt Amtex, Inc. (Burlington, NC) in 1996: 1 510(k) clearance. All are in product code KKX (Drape, Surgical, Antimicrobial). 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 Flynt Amtex, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Flynt Amtex, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Flynt Amtex, 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

Flynt Amtex, Inc.

Which product codes does it file in?

What has FDA decided for it lately?