AURORA TANNING SYSTEMS

GUDID G5100752

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G5100752
• NIH Device Record Key: 9e6ab39a-63fa-4b84-b2b8-7fd48b9bb1e5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AURORA TANNING SYSTEMS
• Version Model Number: 0752
• Company DUNS: 075058495
• Company Name: Light Sources, Inc.
• 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: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G5100752 [Primary]

FDA Product Code

• LEJ: Booth, Sun Tan

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: 2025-08-26
• Device Publish Date: 2025-08-18

On-Brand Devices [AURORA TANNING SYSTEMS]

• G51007020: 0702
• G51007240: FR71T12/BL/BP/6.5
• G5100751: 0751
• G5100752: 0752