FDA applicant

Tridak

Mchenry, IL1 decision1977–19770 recalls

FDA records 1 decision for Tridak (Mchenry, IL) in 1977: 1 510(k) clearance. All are in product code KYX (Dispenser, Liquid Medication). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Tridak since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Tridak”

FDA records each applicant name separately; these may or may not be the same firm.

Tridak Division of Indicon, Inc. 7

Tridak

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Tridak”