KINEON

GUDID 05060981240005

KINEON MOVE+, model: XG-01B, is an over-the-counter light-emitting diode (LED) combined laser-emitting device that emits energy for knee pain relief.

Shenzhen Kaiyan Medical Equipment Co,. Ltd

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• Primary Device ID: 05060981240005
• NIH Device Record Key: 51deb67a-c696-47fe-9d7d-c36f68d5659a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KINEON
• Version Model Number: XG-01B
• Company DUNS: 543062382
• Company Name: Shenzhen Kaiyan Medical Equipment Co,. Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060981240005 [Primary]

FDA Product Code

• ILY: Lamp, Infrared, Therapeutic Heating

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-03
• Device Publish Date: 2023-07-26

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