FDA applicant

Medevice, Inc.

Canada L4w 4m2, CA6 decisions1989–20090 recalls

FDA records 6 decisions for Medevice, Inc. (Canada L4w 4m2, CA) from 1989 to 2009: 6 510(k) clearances. Most are in product codes BSO (Catheter, Conduction, Anesthetic) and KNT (Tubes, Gastrointestinal (And Accessories)). No recall is linked to its devices.

FDA’s records also spell it “Medevice Corporation”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

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

FDA decisions per year

1in 2009

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Medevice, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?