510(k) Report

FDA applicant

Harding Industries, Inc.

Morristown, NJ2 decisions1987–19940 recalls

FDA records 2 decisions for Harding Industries, Inc. (Morristown, NJ) from 1987 to 1994: 2 510(k) clearances. Most are in product codes LRO (General Surgery Tray) and BTQ (Airway, Nasopharyngeal). 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 Harding Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Harding Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Harding”

FDA records each applicant name separately; these may or may not be the same firm.