510(k) Report

FDA applicant

American Container Technology, Inc.

Wallington, NJ3 decisions1986–19870 recalls

FDA records 3 decisions for American Container Technology, Inc. (Wallington, NJ) from 1986 to 1987: 3 510(k) clearances. Most are in product codes FWZ (Operating Room Accessories Table Tray) and HRX (Arthroscope). 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 American Container Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Container Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like American Container Technology, 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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