FDA applicant

Panag International

Johannesburg, ZA1 decision2002–20020 recalls

FDA records 1 decision for Panag International (Johannesburg, ZA) in 2002: 1 510(k) clearance. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Panag International’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Panag International since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Panag International

Which product codes does it file in?

What has FDA decided for it lately?