Scan Post 260-100-630

GUDID 00813110027320

3.0mm Scan Post (2)

BICON, LLC

Dental implant abutment analog, scanning

• Primary Device ID: 00813110027320
• NIH Device Record Key: 99d4b372-c57c-41bc-8978-942e2e337c37
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Scan Post
• Version Model Number: 260-100-630
• Catalog Number: 260-100-630
• Company DUNS: 945015758
• Company Name: BICON, LLC
• Device Count: 2
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813110027320 [Primary]
GS1	10813110027327 [Unit of Use]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-03-25
• Device Publish Date: 2016-05-06

On-Brand Devices [Scan Post]

• 00813110027320: 3.0mm Scan Post (2)
• 00813110027313: 2.5mm Scan Post (2)
• 00813110027306: 2.0mm Scan Post (2)
• 00813110029768: 3.0mm Titanium Scan Post (2)
• 00813110029751: 2.5mm Titanium Scan Post (2)
• 00813110029744: 2.0mm Titanium Scan Post (2)