FDA applicant

Dynamedics, Inc.

London, Ontario, CA3 decisions1987–19950 recalls

FDA records 3 decisions for Dynamedics, Inc. (London, Ontario, CA) from 1987 to 1995: 3 510(k) clearances. Most are in product codes FNM (Mattress, Air Flotation, Alternating Pressure) and INX (Bed, Air Fluidized). No recall is linked to its devices.

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

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

FIG. A — Illustration, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Dynamedics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dynamedics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?