510(k) Report

FDA applicant

American Medical Manufacturer, Inc.

Canoga Park, CA1 decision1993–19930 recalls

FDA records 1 decision for American Medical Manufacturer, Inc. (Canoga Park, CA) in 1993: 1 510(k) clearance. All are in product code FWZ (Operating Room Accessories Table Tray). 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 Medical Manufacturer, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Medical Manufacturer, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like American Medical Manufacturer, 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