Renpho Rejuven

GUDID 00810140062598

LED Light Therapy Mask

Joicom Corporation

Red/blue light phototherapy unit

• Primary Device ID: 00810140062598
• NIH Device Record Key: d24bc4a1-0b1c-4356-9472-5827da6bcac8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Renpho Rejuven
• Version Model Number: E100B
• Company DUNS: 033774836
• Company Name: Joicom Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• Manufacturing Date: false
• 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	00810140062598 [Primary]
GS1	10810140062595 [Package]; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• OLP: Over-The-Counter Powered Light Based Laser For Acne

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: 2025-08-14
• Device Publish Date: 2025-08-06

On-Brand Devices [Renpho Rejuven]

• 10810140062601: LED Light Therapy Mask
• 00810140062598: LED Light Therapy Mask