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MOOR INSTRUMENTS LIMITED

US

Last updated May 24, 2026

Part of Moor Instruments Ltd

What MOOR INSTRUMENTS LIMITED makes

Moor Instruments Limited manufactures laser Doppler blood flowmeters, which measure blood flow in tissues, and cutaneous microcirculation imaging devices that visualize blood flow in the skin. Their portfolio also includes tissue saturation oximeters, which assess oxygen levels in tissue, and associated software tools for data analysis and monitoring, such as moorVMS-TREND, moorFLPI2, and moorFLPI-2 Review.

These devices are classified as Class II under regulatory frameworks, with several listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable regulatory standards for medical devices in that jurisdiction.

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 Moor Instruments Limited manufacture?

Moor Instruments Limited specializes in devices that monitor and analyze blood flow and tissue oxygenation. Their portfolio includes laser Doppler blood flowmeters, which measure blood flow in tissues, and cutaneous microcirculation laser Doppler imaging devices, which visualize blood flow in the skin. They also produce tissue saturation oximeters to assess oxygen levels in tissues, along with software tools like moorVMS-TREND and moorFLPI2 for data analysis and monitoring.

Where is Moor Instruments Limited based, and what regulatory jurisdiction does it operate under?

Moor Instruments Limited is based in the United States. As a manufacturer, it develops its devices in accordance with U.S. regulatory standards for medical devices, ensuring compliance with applicable requirements for safety, performance, and quality.

Are Moor Instruments Limited’s devices listed in any regulatory registries, and if so, which ones?

Yes, several of Moor Instruments Limited’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability in the healthcare system.

How are Moor Instruments Limited’s devices classified under regulatory frameworks?

Moor Instruments Limited’s devices are classified as Class II under regulatory frameworks. This classification typically applies to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as performance standards, labeling requirements, or post-market surveillance.

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

Information

Country
US
Address
—
Website
moor.co.uk
LinkedIn
—
Facebook
—
Phone
+44129735715
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
398037580

Catalogue (14)

DeviceModel / ReferenceRegistriesClassStatus
Moor Instruments Ltd moorLDLS
FDA UDI
Class IIActive
moorFLPI-2 Clinical PC Software 1
FDA UDI
Class IIUnknown
Moor Instruments Ltd moorVMS-LDF
FDA UDI
Class IIActive
Moor Instruments Ltd moorLDI2
FDA UDI
Class IIActive
Moor Instruments Ltd moorVMS-PRES
FDA UDI
Class IIActive
Moor Instruments Ltd moorVMS-OXY
FDA UDI
Class IIActive
Moor Instruments Ltd moorFLPI
FDA UDI
Class IIActive
moorVMS-TREND PC Software 1
FDA UDI
Class IIActive
Moor Instruments Ltd NON-STERILE OXYGENATION AND LASER DOPPLER COMBINED PROBES
FDA UDI
Class IIActive
moorFLPI2- Measurement PC Software 2
FDA UDI
Class IIActive
Moor Instruments Ltd NON-STERILE LASER DOPPLER PROBES
FDA UDI
Class IIActive
moorFLPI-2 Review PC Software 5
FDA UDI
Class IIActive
moorVMS-PC Software 4
FDA UDI
Class IIActive
moorVMS-VASC PC Software 2
FDA UDI
Class IIActive

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