FDA applicant

Contour, Inc.

Walker, MI1 decision1984–19840 recalls

FDA records 1 decision for Contour, Inc. (Walker, MI) in 1984: 1 510(k) clearance. All are in product code LLI (Bed, Therapeutic, Ac-Powered, Adjustable…). 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, general hospital panel, where it files most

How often FDA has decided Contour, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Contour, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Contour, 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 “Contour”

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

Contour Fabricators of Florida, Inc. 18 Contour Medical Technology, Inc. 9 Contour Fabricators, Inc. 8 Contour Electrodes, Inc. 4 Contour Research, LLC 2 Contour Healer, LLC 1 Contour Medical Systems, Inc. 1 Contour Technology 1

Contour, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Contour”