FDA applicant

Mobilife, LLC

Delafield, WI1 decision2006–20060 recalls

FDA records 1 decision for Mobilife, LLC (Delafield, WI) in 2006: 1 510(k) clearance. 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 Mobilife, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mobilife, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mobilife, LLC

Which product codes does it file in?

What has FDA decided for it lately?