FDA applicant

Plainsense Wheelchairs, Inc.

Marietta, GA1 decision2000–20000 recalls

FDA records 1 decision for Plainsense Wheelchairs, Inc. (Marietta, GA) in 2000: 1 510(k) clearance. All are in product code IOR (Wheelchair, Mechanical). 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 Plainsense Wheelchairs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Plainsense Wheelchairs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Plainsense Wheelchairs, Inc.

Which product codes does it file in?

What has FDA decided for it lately?