FDA applicant

Motion Lab Systems, Inc.

Baton Rouge, LA2 decisions1998–20000 recalls

FDA records 2 decisions for Motion Lab Systems, Inc. (Baton Rouge, LA) from 1998 to 2000: 2 510(k) clearances. All are in product code IKN (Electromyograph, Diagnostic). Its devices cite 1 predicate, 0 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 Lab Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Motion Lab Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Motion”

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

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

Motion Lab Systems, Inc.

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”