510(k) Report

FDA applicant

Innovative Technology, Ltd.

Ontario L3y 1j8, CA2 decisions1992–19930 recalls

FDA records 2 decisions for Innovative Technology, Ltd. (Ontario L3y 1j8, CA) from 1992 to 1993: 2 510(k) clearances. Most are in product codes MGP (Dressing, Wound And Burn, Occlusive) and JEP (Retainer, Matrix). 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, dental panel, where it files most

How often FDA has decided Innovative Technology, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Innovative Technology, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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