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Fujian Meo Medical Technology Limited

US

Last updated May 24, 2026

Part of Fujian Meo Medical Technology Ltd.

What Fujian Meo Medical Technology Limited makes

Fujian Meo Medical Technology Limited manufactures single-use surgical and medical face masks designed for healthcare settings. These products are intended for patient and user protection during medical procedures to reduce airborne contamination.

The company’s portfolio is regulated as Class II devices under FDA pathways, including 510(k) clearance and UDI compliance. These products are listed in the FDA’s regulatory databases. The manufacturer is based in the US.

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 Fujian Meo Medical Technology Limited manufacture?

Fujian Meo Medical Technology Limited specializes in single-use surgical and medical face masks. These masks are designed for healthcare environments to protect both patients and healthcare providers from airborne contaminants during medical procedures. The focus is on disposable masks, ensuring hygiene and safety in clinical settings.

Where is Fujian Meo Medical Technology Limited based?

The company is based in the United States. This location allows it to comply with US regulatory requirements, including those for medical devices like surgical and medical face masks.

Which regulatory registries or databases list Fujian Meo Medical Technology Limited’s devices?

Fujian Meo Medical Technology Limited’s devices are listed in the FDA’s regulatory databases, specifically under the 510(k) clearance pathway and the Unique Device Identifier (UDI) system. These registries ensure traceability and compliance with US medical device regulations.

How are Fujian Meo Medical Technology Limited’s devices classified under FDA regulations?

The company’s devices, such as single-use surgical and medical face masks, are classified as Class II under FDA regulations. This classification typically applies to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness.

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

Information

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US
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Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Meo 17.5×9.5
FDA UDI
Class IIActive
MEO Med Disposable Medical Face Mask K210870
FDA 510(k)
Class IIActive

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