510(k) Report

FDA applicant

Ttk Protective Devices Limited (Formerly Ttk-Lig L

Aurora, IL1 decision2014–20140 recalls

FDA records 1 decision for Ttk Protective Devices Limited (Formerly Ttk-Lig L (Aurora, IL) in 2014: 1 510(k) clearance. All are in product code HIS (Condom). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Ttk Protective Devices Limited (Formerly Ttk-Lig L’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2014: 1
2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Ttk Protective Devices Limited (Formerly Ttk-Lig L by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • HISCondom1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K132490Skore and Multiple BrandsTtk Protective Devices Limited (Formerly Ttk-Lig L · 20141cites it

What has FDA decided for it lately?

  • K132490Skore and Multiple BrandsTtk Protective Devices Limited (Formerly Ttk-Lig L · 2014

The one decision as Ttk Protective Devices Limited (Formerly Ttk-Lig L →