FDA applicant

Escalon Medical Trek

Mukwonago, WI1 decision1992–19920 recalls

FDA records 1 decision for Escalon Medical Trek (Mukwonago, WI) in 1992: 1 510(k) clearance. All are in product code BXX (Calibrator, Pressure, Gas). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Escalon Medical Trek since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Escalon Medical Trek 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 Trek Medical 3

Escalon Medical Trek

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Escalon”