FDA applicant

Fortress Scientific, Ltd.

Washington, DC27 decisions1989–19940 recalls

FDA records 27 decisions for Fortress Scientific, Ltd. (Washington, DC) from 1989 to 1994: 27 510(k) clearances. Most are in product codes ITI (Wheelchair, Powered) and INI (Vehicle, Motorized 3-Wheeled). 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 Scientific, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fortress Scientific, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Fortress”

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

Fortress Litestyle 8 Fortress Lite-Style Wheelchairs, Inc. 3 Fortress, Inc. 2

Fortress Scientific, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Fortress”