FDA applicant

Trek Medical Products, Inc.

Muckwonago, WI8 decisions1986–19920 recalls

FDA records 8 decisions for Trek Medical Products, Inc. (Muckwonago, WI) from 1986 to 1992: 8 510(k) clearances. Most are in product codes HQE (Instrument, Vitreous Aspiration And Cutting…) and FST (Light, Surgical, 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, ophthalmic panel, where it files most

How often FDA has decided Trek Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Trek Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Trek”

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

Trek Diagnostic Systems, Inc. 69

Trek Medical Products, Inc.

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?

Other applicant names beginning “Trek”