FDA applicant

Dryden Corp.

Mchenry, IL21 decisions1976–19880 recalls

FDA records 21 decisions for Dryden Corp. (Mchenry, IL) from 1976 to 1988: 21 510(k) clearances. Most are in product codes CAI (Circuit, Breathing (W Connector, Adaptor, Y…) and BZO (Set, Tubing And Support, Ventilator (W Harness)). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Dryden Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dryden 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?