RENUVATAN

GUDID G5103275

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G5103275
• NIH Device Record Key: 7caf8ab6-9940-49b5-afd1-275de3ba8d62
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENUVATAN
• Version Model Number: 3275
• 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	G5103275 [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: 2024-12-19
• Device Publish Date: 2024-12-11

Devices Manufactured by Light Sources, Inc.

• G5102842 - COSMETTA: 2024-12-27
• G5103169 - Pro tech ll: 2024-12-26
• G51023810 - HEARTLAND: 2024-12-25
• G5102483 - AUVL: 2024-12-25
• G51029960 - SUN ANGEL: 2024-12-25
• G5103046 - GENESIS: 2024-12-25
• G51017960 - UV POWER: 2024-12-20
• G51028990 - NEW TECHNOLOGY: 2024-12-20