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Ningbo Wise Optomech Technology Corporation

US

Last updated May 30, 2026

Part of Ningbo Wise Optomech Technology Corporation

What Ningbo Wise Optomech Technology Corporation makes

Ningbo Wise Optomech Technology Corporation manufactures endoscopic video image processing units, including systems designed for real-time imaging in medical procedures. Their portfolio includes devices like the WiScope®, which enhance visual clarity and functionality during endoscopic examinations.

The company’s products are classified as Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 Ningbo Wise Optomech Technology Corporation manufacture?

Ningbo Wise Optomech Technology Corporation specializes in endoscopic video image processing units. These devices are designed to improve real-time imaging during medical procedures, such as endoscopic examinations, by enhancing visual clarity and functionality. The company’s portfolio includes systems like the WiScope®, which are tailored for use in minimally invasive surgeries and diagnostic procedures.

Where is Ningbo Wise Optomech Technology Corporation based?

The company operates from the United States. While its name suggests origins in Ningbo, China, its current headquarters and primary business operations are located within the US market.

Which regulatory registries list devices manufactured by Ningbo Wise Optomech Technology Corporation?

Devices produced by Ningbo Wise Optomech Technology Corporation are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the US, ensuring transparency and traceability in the healthcare supply chain.

How are the devices made by Ningbo Wise Optomech Technology Corporation classified under medical device regulations?

The company’s devices, such as the WiScope® endoscopic video image processing units, fall under Class II classification. This classification is determined based on factors like the risk associated with the device’s use, its intended purpose, and the potential harm if it malfunctions. Class II devices typically require special controls in addition to general controls to ensure safety and effectiveness.

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

Information

Country
US
Address
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Website
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LinkedIn
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Email
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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
540094524

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
WiScope® OTU-A
FDA UDI
Class IIActive
WiScope® OTU-A
FDA UDI
Class IIActive

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