ossFX

GUDID 00812593021580

ossFX Fusion Kit

Biogennix, LLC

Synthetic bone graft

• Primary Device ID: 00812593021580
• NIH Device Record Key: 1045c296-0672-4a0c-a4a0-1e07da660168
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ossFX
• Version Model Number: AXB-OSF-11
• Company DUNS: 832270370
• Company Name: Biogennix, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812593021580 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093342

FDA Product Code

• MQV: Filler, Bone Void, Calcium Compound

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: 2023-12-21
• Device Publish Date: 2023-12-13

On-Brand Devices [ossFX]

• 00812593021610: ossFX 12cc
• 00812593021603: ossFX 6cc
• 00812593021597: ossFX 3cc
• 00812593021580: ossFX Fusion Kit