FDA applicant

Stickman Industries, Inc.

Ottawa, Ontario, CA1 decision2002–20020 recalls

FDA records 1 decision for Stickman Industries, Inc. (Ottawa, Ontario, CA) in 2002: 1 510(k) clearance. All are in product code MLW (Warmer, Peritoneal Dialysate). 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 Stickman Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Stickman Industries, Inc.

Which product codes does it file in?

What has FDA decided for it lately?