FDA applicant

Probed Medical Technologies, Inc.

Chilliwack, B.C., CA1 decision1996–19960 recalls

FDA records 1 decision for Probed Medical Technologies, Inc. (Chilliwack, B.C., CA) in 1996: 1 510(k) clearance. All are in product code IKZ (Bed, Patient Rotation, Powered). 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 Probed Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Probed Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Probed Medical Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?