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MAXQ AI LTD

US

Last updated May 30, 2026

What MAXQ AI LTD makes

MAXQ AI LTD produces medical software, specifically Radiology DICOM image processing application software, such as AccipioIx. This software is used for processing medical images. The company's products are related to radiology and medical imaging.

The company's portfolio is regulated as Class II devices and is listed in the FDA UDI registry. The devices are subject to regulatory oversight in the US, where the company is based.

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

Frequently asked questions

What does MAXQ AI LTD make?

MAXQ AI LTD produces medical software, specifically Radiology DICOM image processing application software, such as AccipioIx. This software is used for processing medical images and is related to radiology and medical imaging. The company's portfolio consists of these types of devices, which are regulated as Class II products.

Where is MAXQ AI LTD based?

MAXQ AI LTD is based in the United States (US), as indicated in the company's country field. The company operates from this location, and its devices are subject to regulatory oversight in the US, where it is headquartered.

Which regulatory registries list MAXQ AI LTD's devices?

MAXQ AI LTD's devices are listed in the FDA UDI registry, as specified in the LISTED IN field. This registry contains information about the company's medical devices, including their unique device identifiers, and is used for tracking and regulatory purposes in the United States.

How are MAXQ AI LTD's devices classified?

MAXQ AI LTD's devices are classified as Class II, as stated in the DEVICE CLASSES field. This classification indicates that the devices require special controls to ensure safety and effectiveness, and they are subject to regulatory requirements appropriate for moderate-risk medical devices.

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

Information

Country
US
Address
—
Website
maxq.ai
LinkedIn
—
Facebook
—
Phone
+1-617-765-0333
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
600570388

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
AccipioIx V1.6
FDA UDI
Class IIActive
AccipioIx V2.3 and subsequent minor V2.x releases
FDA UDI
Class IIActive

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