PLENA Graft 1.0

GUDID 00813954024660

Anorganic Bone Mineral 1.0cc (0.25-1mm)

COLLAGEN MATRIX, INC.

Dental bone matrix implant, animal-derived

• Primary Device ID: 00813954024660
• NIH Device Record Key: 666e6025-6587-462b-a66e-340ff3ab12c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PLENA Graft 1.0
• Version Model Number: PMC1010
• Company DUNS: 176262442
• Company Name: COLLAGEN MATRIX, 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: 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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813954024660 [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: 2022-03-21
• Device Publish Date: 2022-03-11

On-Brand Devices [PLENA Graft 1.0]

• 00813954024660: Anorganic Bone Mineral 1.0cc (0.25-1mm)
• 00813954027029: Anorganic Bone Mineral