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ContourMD Marketing Group, LLC

US

Last updated May 24, 2026

What ContourMD Marketing Group, LLC makes

The company produces non-gel, non-antimicrobial exudate-absorbent dressings designed for wound care, as well as pressure-relieving cushions for the perineal, coccygeal, and lumbar regions. These products are intended to manage moisture and reduce pressure-related discomfort in clinical and home settings.

All listed devices fall under Class I regulation in the US and are registered in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable regulatory standards for these categories.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does ContourMD Marketing Group, LLC manufacture?

ContourMD Marketing Group, LLC specializes in two primary categories of medical devices: non-gel, non-antimicrobial exudate-absorbent dressings for wound care and pressure-relieving cushions. The cushions are designed for specific areas like the perineal, coccygeal, and lumbar regions to help manage moisture and reduce pressure-related discomfort in both clinical and home settings.

Where is ContourMD Marketing Group, LLC based?

The company is based in the United States. This location ensures compliance with US regulatory standards, which govern the design, manufacturing, and distribution of their medical devices.

Which regulatory registries list ContourMD Marketing Group, LLC’s devices?

ContourMD Marketing Group, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their products under US regulatory oversight.

How are ContourMD Marketing Group, LLC’s devices classified under US regulations?

All of ContourMD Marketing Group, LLC’s devices fall under Class I regulation in the US. This classification applies to low-risk medical devices, such as exudate-absorbent dressings and pressure-relieving cushions, which are deemed to pose minimal risk to patients when used as intended.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
contourmd.com
LinkedIn
—
Facebook
—
Phone
913-541-9200
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
147299259

Catalogue (9)

DeviceModel / ReferenceRegistriesClassStatus
ContourMD Purchased: LIP-02-BBL
FDA UDI
Class IActive
ContourMD LIP-03-BBL
FDA UDI
Class IActive
ContourMD LIP-03
FDA UDI
Class IActive
ContourMD LIP-01
FDA UDI
Class IActive
ContourMD Purchased:CMD-LUMBB-0S
FDA UDI
Class IActive
ContourMD LIP-01-ABBD
FDA UDI
Class IActive
ContourMD LIP-02
FDA UDI
Class IActive
ContourMD LIP-01-NB
FDA UDI
Class IActive
ContourMD LIPO-10
FDA UDI
Class IActive

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