FDA applicant

Motion Composites

Saint-Roch-De-L' Achigan, CA4 decisions2012–20260 recalls

FDA records 4 decisions for Motion Composites (Saint-Roch-De-L' Achigan, CA) from 2012 to 2026: 4 510(k) clearances. All are in product code IOR (Wheelchair, Mechanical). Its devices cite 9 predicates, 4 of them its own earlier devices. 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 Motion Composites’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Motion Composites by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Motion Composites’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Motion”

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

Motion Concepts 9 Motion Designs, Inc. 4 Motion Analysis Corp. 4 Motion Control, Inc. 4 Motion Lab Systems, Inc. 2 Motion Dynamics 1 Motion Manufacturers, Inc. 1 Motion Medical Products, LLC 1 Motion Media Technology, Inc. 1 Motion Informatics ltd. 1

Motion Composites

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Motion”