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Wuhan PHOMED Technology Company , Ltd.

US

Last updated May 23, 2026

What Wuhan PHOMED Technology Company , Ltd. makes

Wuhan PHOMED Technology Company, Ltd. manufactures non-wearable musculoskeletal infrared phototherapy units, including the DIOWAVE and CureLight Medical Diode Laser Systems such as CureLight F2-A15, CureLight F2-B15, CureLight F2-A30, CureLight F2-B30, CureLight F3-AB30, and CureLight F3-AB60.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. The company is based in 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 type of medical devices does Wuhan PHOMED Technology Company, Ltd. manufacture?

Wuhan PHOMED Technology Company, Ltd. manufactures non-wearable musculoskeletal infrared phototherapy units, as stated in the device data. These include specific product lines such as the DIOWAVE and CureLight Medical Diode Laser Systems, which are examples of the devices they produce. The company focuses on this category of devices for therapeutic use in musculoskeletal applications.

Where is Wuhan PHOMED Technology Company, Ltd. based?

The company is based in the United States, as explicitly indicated in the device data under the COUNTRY field. This information is provided directly in the summary and metadata, confirming the location of the company’s operations or registration.

In which regulatory registries are the devices from Wuhan PHOMED Technology Company, Ltd. listed?

The devices manufactured by Wuhan PHOMED Technology Company, Ltd. are listed in the FDA 510(k) and FDA UDI registries, as specified in the LISTED IN field of the device data. These registries are used to track medical devices that have undergone premarket notification and unique device identification requirements in the United States.

How are the devices from Wuhan PHOMED Technology Company, Ltd. classified?

The devices are classified as Class II medical devices, as stated in the DEVICE CLASSES field of the device data. This classification indicates that these devices require special controls to ensure safety and effectiveness, but do not require premarket approval like Class III devices.

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

Information

Country
US
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Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Diowave 250WLS
FDA UDI
Class IIActive
Diowave 100WLS
FDA UDI
Class IIActive
CureLight Medical Diode Laser Systems (CureLight F2-A15; CureLight F2-B15; CureLight F2-A30; CureLight F2-B30; CureLight F3-AB30; CureLight F3-AB60.) K253965
FDA 510(k)
Class IIActive

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