FDA applicant

Fortress, Inc.

Washington, DC2 decisions1990–19900 recalls

FDA records 2 decisions for Fortress, Inc. (Washington, DC) in 1990: 2 510(k) clearances. All are in product code ITI (Wheelchair, Powered). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Fortress, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Fortress, 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 “Fortress”

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

Fortress Scientific, Ltd. 27 Fortress Litestyle 8 Fortress Lite-Style Wheelchairs, Inc. 3

Fortress, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Fortress”