Screw 260-100-023

GUDID 00813110029546

Mesh Retention Screw (2)

BICON, LLC

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 00813110029546
• NIH Device Record Key: 06d9df13-7ee3-464a-96e1-204bac885c06
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Screw
• Version Model Number: 260-100-023
• Catalog Number: 260-100-023
• Company DUNS: 945015758
• Company Name: BICON, 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: 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
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com
• Phone: 617-524-4443
• Email: support@bicon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813110029546 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

[00813110029546]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-11
• Device Publish Date: 2023-07-03

Devices Manufactured by BICON, LLC

• 00813110027276 - Universal Abutment: 2024-10-29 Universal Abutment UA6 SP 0° - 3.0mm Tall Post
• 00813110027283 - Universal Abutment: 2024-10-29 Universal Abutment UA6 SP 15° - 3.0mm Tall Post
• 00813110029744 - Scan Post: 2024-10-29 2.0mm Titanium Scan Post (2)
• 00813110029751 - Scan Post: 2024-10-29 2.5mm Titanium Scan Post (2)
• 00813110029768 - Scan Post: 2024-10-29 3.0mm Titanium Scan Post (2)
• 00813110029775 - Temporary Abutment: 2024-10-29 6.5 x 4.5mm Scannable Temporary Abutment - 3.0mm Tall Post
• 00813110029669 - Temporary Abutment: 2024-08-13 4.0 x 6.5mm Scannable Temporary Abutment - 3.0mm Post
• 00813110029676 - Temporary Abutment: 2024-08-13 4.0 x 4.5mm Scannable Temporary Abutment - 3.0mm Tall Post