FDA applicant

Trylon Corp.

Torrance, CA7 decisions1995–20041 recall

FDA records 7 decisions for Trylon Corp. (Torrance, CA) from 1995 to 2004: 7 510(k) clearances. Most are in product codes MPU (Source, Chemiluminescent Light) and EAZ (Light, Operating, Dental). Its devices cite 2 predicates, 2 of them its own earlier devices. 1 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Trylon Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Trylon”

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

Trylon Associates, Ltd. 1

Trylon 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?

What has been recalled?

Other applicant names beginning “Trylon”