FDA applicant

The Washington Group, Inc.

Dallas, TX1 decision1984–19840 recalls

FDA records 1 decision for The Washington Group, Inc. (Dallas, TX) in 1984: 1 510(k) clearance. All are in product code KNT (Tubes, Gastrointestinal (And Accessories)). 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 The Washington Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Washington Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Washington Group, 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

Other applicant names beginning “The”

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

Washington-Greene County Branch Pennsylvania Assoc 3 Washington Regulatory Services 3 Washington Biotechnology 1 Washington Biolab, Inc. 1

The Washington Group, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”