FDA applicant

Dymax Corp

Pittsburgh, PA7 decisions1985–20030 recalls

FDA records 7 decisions for Dymax Corp (Pittsburgh, PA) from 1985 to 2003: 7 510(k) clearances. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and DQY (Catheter, Percutaneous). Its devices cite 4 predicates, 4 of them its own earlier devices. 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Dymax Corp since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dymax Corp

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?