510(k) Report

FDA applicant

Global TV Concepts, Ltd.

Washington, DC3 decisions1997–20020 recalls

FDA records 3 decisions for Global TV Concepts, Ltd. (Washington, DC) from 1997 to 2002: 3 510(k) clearances. Most are in product codes KCX (Epilator, High Frequency, Tweezer-Type) and IMC (Bath, Paraffin). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Global TV Concepts, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Global TV Concepts, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Global TV Concepts, Ltd.’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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