FDA applicant

Rehab 'N Motion Technologies

Breda, NL1 decision1995–19950 recalls

FDA records 1 decision for Rehab 'N Motion Technologies (Breda, NL) in 1995: 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 Rehab 'N Motion Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rehab 'N Motion Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rehab 'N Motion Technologies by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Rehab”

FDA records each applicant name separately; these may or may not be the same firm.

Rehab Technology, Inc. 4 Rehab Medical Specialties, Inc. 3 Rehab, Inc. 1

Rehab 'N Motion Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Rehab”