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Wide Corporation

US

Last updated May 30, 2026

What Wide Corporation makes

Wide Corporation manufactures colour image display units, including medical-grade monitors with varying resolutions such as 2MP, 6MP, and TFT LCD systems. These devices are designed for integration with imaging interfaces, such as the WIDE 2MP TFT LCD Monitor System IF 1902A, and support clinical display applications in healthcare settings.

The company’s products fall under FDA Class II medical devices and are authorised through the 510(k) and UDI pathways. These devices are listed in the FDA’s regulatory databases, and the manufacturer operates from the United States.

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 Wide Corporation manufacture?

Wide Corporation specializes in producing colour image display units, specifically medical-grade monitors. These include devices with varying resolutions such as 2MP, 6MP, and TFT LCD systems, often designed for integration with imaging interfaces like the WIDE 2MP TFT LCD Monitor System IF 1902A. Their focus is on clinical display applications used in healthcare settings.

Where is Wide Corporation based?

Wide Corporation is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and compliance with US-based medical device standards.

Which regulatory registries list Wide Corporation’s devices?

Wide Corporation’s devices are listed in the FDA’s regulatory databases under the 510(k) and UDI (Unique Device Identification) pathways. These registries ensure traceability and compliance tracking for Class II medical devices authorised in the US.

How are Wide Corporation’s devices classified by regulatory authorities?

Wide Corporation’s devices fall under FDA Class II classification. This classification is determined by the risk associated with the device, where Class II devices require special controls to ensure safety and effectiveness beyond general controls, such as the 510(k) premarket notification process.

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

Information

Country
US
Address
—
Website
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LinkedIn
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Facebook
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Email
—
Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
688285899

Catalogue (31)

DeviceModel / ReferenceRegistriesClassStatus
Mx50n MX50YQS
FDA UDI
Class IIActive
Cx30n CX30PQX
FDA UDI
Class IIActive
Cx50n CX50YQS
FDA UDI
Class IIActive
Mx50t MX50TQS
FDA UDI
Class IIActive
Mx30n MX30TQS
FDA UDI
Class IIActive
Cx30n CX30PQX
FDA UDI
Class IIActive
Cx50n CX50YQS
FDA UDI
Class IIActive
Cw120n CW120N
FDA UDI
Class IIActive
6mp CW60
FDA UDI
Class IIActive
Mx50n MX50YQS
FDA UDI
Class IIActive
Cx20n CX20PUX
FDA UDI
Class IIActive
Wide 2mp Tft Lcd Monitor System If 1902a K032960
FDA 510(k)
Class IIActive
5mp Tft Lcd Monitor System If2105a By Wide Corporation K031929
FDA 510(k)
Class IIActive
Cx50n(cx50yqs) K170783
FDA 510(k)
Class IIActive
Mw100 (mammography) Lcd Monitor System K110596
FDA 510(k)
Class IIActive
Wide 5mp (mammo) Lcd Monitor System K052312
FDA 510(k)
Class IIActive
Wide 1mp Lcd Monitor System K042634
FDA 510(k)
Class IIActive
Cl24n K222717
FDA 510(k)
Class IIActive
Cw60n K222722
FDA 510(k)
Class IIActive
Cw120n K210491
FDA 510(k)
Class IIActive
Mx50n(mx50yqs) K160353
FDA 510(k)
Class IIActive
Cx30n (cx30pqx) K210493
FDA 510(k)
Class IIActive
Mx50t(mx50tqs) K160354
FDA 510(k)
Class IIActive
Mx50n K222716
FDA 510(k)
Class IIActive
Cx30n (cx30pqx) K160348
FDA 510(k)
Class IIActive
Mx50n(mx50yqs) K170781
FDA 510(k)
Class IIActive
Mx30n(mx30tqs) K160346
FDA 510(k)
Class IIActive
Cx20n(cx20pux) K160355
FDA 510(k)
Class IIActive
Wide 3mp Grayscale Tft Lcd Monitor If2103a K032174
FDA 510(k)
Class IIActive
Cx50n K222719
FDA 510(k)
Class IIActive
Cx50n, Cx50yqs K160351
FDA 510(k)
Class IIActive

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