510(k) Report

FDA applicant

Mcconnell Orthopedic

Dallas, TX16 decisions1987–19910 recalls

FDA records 16 decisions for Mcconnell Orthopedic (Dallas, TX) from 1987 to 1991: 16 510(k) clearances. Most are in product codes FWZ (Operating Room Accessories Table Tray) and HTO (Reamer). 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 Mcconnell Orthopedic’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mcconnell Orthopedic since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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