Agilon Surgical Collagen+

GUDID 00812593023027

Biogennix, LLC

Animal-derived wound matrix dressing

• Primary Device ID: 00812593023027
• NIH Device Record Key: b90b1f41-4e50-4270-8895-aa073c89e5fc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Agilon Surgical Collagen+
• Version Model Number: ASC-050
• Company DUNS: 832270370
• Company Name: Biogennix, LLC
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	00812593023027 [Primary]

FDA Product Code

• KGN: Wound Dressing With Animal-Derived Material(S)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-04-01
• Device Publish Date: 2026-03-24

On-Brand Devices [Agilon Surgical Collagen+]

• 00812593023027: ASC-050
• 00812593023010: ASC-025