FDA applicant

Escalon Trek Medical

Mukwonago, WI3 decisions1992–19960 recalls

FDA records 3 decisions for Escalon Trek Medical (Mukwonago, WI) from 1992 to 1996: 3 510(k) clearances. Most are in product codes KYG (Device, Irrigation, Ocular Surgery) and MPA (Endoilluminator). 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 Escalon Trek Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Escalon Trek Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Escalon”

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

Escalon Medical Corp. 3 Escalon Medical Trek 1

Escalon Trek Medical

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 “Escalon”