510(k) Report

FDA applicant

Progress Mankind Technology

Hopkins, MN17 decisions1980–19880 recalls

FDA records 17 decisions for Progress Mankind Technology (Hopkins, MN) from 1980 to 1988: 17 510(k) clearances. Most are in product codes GZL (Electrode, Depth) and HAX (Tong, Skull For Traction). 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, neurology panel, where it files most

How often FDA has decided Progress Mankind Technology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Progress Mankind Technology since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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