FDA applicant

Fortress Litestyle

Washington, DC8 decisions1991–19910 recalls

FDA records 8 decisions for Fortress Litestyle (Washington, DC) in 1991: 8 510(k) clearances. Most are in product codes IOR (Wheelchair, Mechanical) and 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 Litestyle’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fortress Litestyle since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fortress Litestyle 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 Scientific, Ltd. 27 Fortress Lite-Style Wheelchairs, Inc. 3 Fortress, Inc. 2

Fortress Litestyle

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Fortress”