510(k) Report

FDA applicant

Morgan Medical Co.

Columbus, GA2 decisions1994–20020 recalls

FDA records 2 decisions for Morgan Medical Co. (Columbus, GA) from 1994 to 2002: 2 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and BZG (Spirometer, Diagnostic). No recall is linked to its devices.

FDA’s records also spell it “Morgan Medical , Ltd.”.

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 Morgan Medical Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Morgan Medical Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Morgan Medical Co.’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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Other applicant names beginning “Morgan”

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