FDA applicant

Trylon Associates, Ltd.

Harbor City, CA1 decision1985–19850 recalls

FDA records 1 decision for Trylon Associates, Ltd. (Harbor City, CA) in 1985: 1 510(k) clearance. All are in product code HIC (Speculum, Vaginal, Nonmetal, Fiberoptic). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Trylon Associates, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Trylon Associates, Ltd. 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 Corp. 7

Trylon Associates, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Trylon”