Soper Brothers Custom

GUDID PROSV2623

Soper Brothers, Incorporated

Eyeball prosthesis, custom-made

• Primary Device ID: PROSV2623
• NIH Device Record Key: cd42de00-f1b8-4a49-af34-62ea0cdfedfb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Soper Brothers Custom
• Version Model Number: 1
• Company DUNS: 008094807
• Company Name: Soper Brothers, Incorporated
• 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: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: true
• 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
HIBCC	PROSV2623 [Primary]

FDA Product Code

• HQH: Eye, Artificial, Non-Custom

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: 2026-03-11
• Device Publish Date: 2026-03-03

On-Brand Devices [Soper Brothers Custom]

• SHELLV2627: 1
• PROSV2623: 1
• CONFV2628: 1