FDA applicant

Jordco, Inc.

Beaverton, OR2 decisions1994–19990 recalls

FDA records 2 decisions for Jordco, Inc. (Beaverton, OR) from 1994 to 1999: 2 510(k) clearances. Most are in product codes KCT (Sterilization Wrap Containers, Trays…) and KJJ (Cleanser, Root Canal). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Jordco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Jordco, Inc.’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

Jordco, Inc.

Which product codes does it file in?

What has FDA decided for it lately?