InterOss Collagen

GUDID 00852072007421

SIGMAGRAFT, INC.

Dental bone matrix implant, animal-derived

• Primary Device ID: 00852072007421
• NIH Device Record Key: 66555423-0e52-4097-9aac-9a8a84881295
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: InterOss Collagen
• Version Model Number: IOC-050
• Company DUNS: 078893672
• Company Name: SIGMAGRAFT, INC.
• 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: true
• Manufacturing Date: true
• 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	00852072007421 [Primary]

FDA Product Code

• NPM: Bone Grafting Material, Animal Source

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: 2023-05-23
• Device Publish Date: 2023-05-15

On-Brand Devices [InterOss Collagen]

• 00852072007506: IOC-P450
• 00852072007490: IOC-P400
• 00852072007483: IOC-P250
• 00852072007476: IOC-P150
• 00852072007469: IOC-500
• 00852072007452: IOC-350
• 00852072007445: IOC-250
• 00852072007438: IOC-100
• 00852072007421: IOC-050