FDA applicant

Contour Medical Technology, Inc.

Lavergne, TN9 decisions1996–19971 recall

FDA records 9 decisions for Contour Medical Technology, Inc. (Lavergne, TN) from 1996 to 1997: 9 510(k) clearances. Most are in product codes FMT (Warmer, Infant Radiant) and MKJ (Automated External Defibrillators (Non-Wearable)). 1 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 Medical Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Contour Medical Technology, Inc. since 2007.

Recalls per year

1in 2015

2007high 1 (2015) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Contour Medical Technology, 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 Fabricators, Inc. 8 Contour Electrodes, Inc. 4 Contour Research, LLC 2 Contour, Inc. 1 Contour Healer, LLC 1 Contour Medical Systems, Inc. 1 Contour Technology 1

Contour Medical Technology, 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?

What has been recalled?

Other applicant names beginning “Contour”