Solawave

GUDID 06956822893037

Solawave eye recovery pro

Shenzhen Goodwind technology development Co.,Ltd

Red/infrared light phototherapy unit

• Primary Device ID: 06956822893037
• NIH Device Record Key: e2902b7c-99ce-4ef9-8d50-0535355fab05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Solawave
• Version Model Number: PH-e03
• Company DUNS: 527169769
• Company Name: Shenzhen Goodwind technology development 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06956822893037 [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: 2026-02-12
• Device Publish Date: 2026-02-04

On-Brand Devices [Solawave]

• 06956822893037: Solawave eye recovery pro
• 06956822893020: Solawave Neck & Chest Pro Light Therapy Mask
• 06956822893013: Solawave Wrinkle Retreat Pro Light Therapy Face Mask