510(k) Report

FDA applicant

Per4max Medical, LLC

Grand Prairie, TX1 decision2003–20030 recalls

FDA records 1 decision for Per4max Medical, LLC (Grand Prairie, TX) in 2003: 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 Per4max Medical, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Per4max Medical, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Per4max Medical, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IORWheelchair, Mechanical1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K032123Shockwave Suspension WheelchairPer4max Medical, LLC · 20032cite it

What has FDA decided for it lately?

  • K032123Shockwave Suspension WheelchairPer4max Medical, LLC · 2003

The one decision as Per4max Medical, LLC →