FDA applicant

Runch Group USA, Inc.

Houston, TX1 decision1998–19980 recalls

FDA records 1 decision for Runch Group USA, Inc. (Houston, TX) in 1998: 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 Runch Group USA, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Runch Group USA, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Runch Group USA, Inc.

Which product codes does it file in?

What has FDA decided for it lately?