FDA applicant

Turbo Wheelchair Co., Inc.

Beaufort, SC2 decisions2003–20240 recalls

FDA records 2 decisions for Turbo Wheelchair Co., Inc. (Beaufort, SC) from 2003 to 2024: 2 510(k) clearances. 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 Turbo Wheelchair Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2007high 1 (2024) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Turbo Wheelchair Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?