ULTRA BRONZER 200R

GUDID G51032080

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G51032080
• NIH Device Record Key: cdb5bed6-15e0-46d4-a014-1d73a8f57727
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ULTRA BRONZER 200R
• Version Model Number: 3208
• 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	G51032080 [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: 2025-02-18
• Device Publish Date: 2025-02-10

Devices Manufactured by Light Sources, Inc.

• G5103194 - RENUVASKIN: 2025-03-04
• G51032910 - GENESIS: 2025-03-04
• G5101490 - CHEETAH: 2025-03-03
• G5102376 - TAN AMERICA: 2025-03-03
• G5102557 - GENESIS: 2025-03-03
• G5102845 - COSMETTA: 2025-03-03
• G5101089 - GENESIS: 2025-02-28
• G5101970 - BRILLIANCE ACTIVE BRONZER: 2025-02-28