FDA applicant

Wallant Intl. Trade, Inc.

Roselle, NJ3 decisions1981–19860 recalls

FDA records 3 decisions for Wallant Intl. Trade, Inc. (Roselle, NJ) from 1981 to 1986: 3 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and GXY (Electrode, Cutaneous). 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 Wallant Intl. Trade, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wallant Intl. Trade, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Wallant Intl. Trade, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Wallant Intl. Trade, Inc.

Which product codes does it file in?

What has FDA decided for it lately?