510(k) Report

FDA applicant

Tech-Cons Ltd., Intl.

Mchenry, IL6 decisions1984–19840 recalls

FDA records 6 decisions for Tech-Cons Ltd., Intl. (Mchenry, IL) in 1984: 6 510(k) clearances. Most are in product codes KOD (Catheter, Urological) and KNX (Collector, Urine, (And Accessories) For…). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Tech-Cons Ltd., Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tech-Cons Ltd., Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tech-Cons Ltd., Intl. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Tech-Cons Ltd., Intl.’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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