510(k) Report

FDA applicant

Lsl Industries, Inc.

Mchenry, IL2 decisions1983–19890 recalls

FDA records 2 decisions for Lsl Industries, Inc. (Mchenry, IL) from 1983 to 1989: 2 510(k) clearances. Most are in product codes KTC (Bath, Sitz, Nonpowered) and EYZ (System, Urine Drainage, Closed, 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, physical medicine panel, where it files most

How often FDA has decided Lsl Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lsl Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Lsl Industries, Inc.’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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