FDA applicant

Pathfinder Intl. Corp.

Jacksonville, FL2 decisions1984–19930 recalls

FDA records 2 decisions for Pathfinder Intl. Corp. (Jacksonville, FL) from 1984 to 1993: 2 510(k) clearances. Most are in product codes KNX (Collector, Urine, (And Accessories) For…) and KNN (Components, Wheelchair). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Pathfinder Intl. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pathfinder Intl. Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Pathfinder”

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

Pathfinder Therapeutics, Inc. 4 Pathfinder Cell Therapy, Inc. 1

Pathfinder Intl. Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pathfinder”