LO 260-300-502

GUDID 00813110028228

2.0mm LO Abutment - 3.0mm Post

BICON, LLC

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed

• Primary Device ID: 00813110028228
• NIH Device Record Key: 697ec959-c4c9-43f5-b0ba-d6685aca2805
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LO
• Version Model Number: 260-300-502
• Catalog Number: 260-300-502
• Company DUNS: 945015758
• Company Name: BICON, 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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813110028228 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K853788

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-08
• Device Publish Date: 2019-09-01

On-Brand Devices [LO]

• 00813110028259: 5.0mm LO Abutment - 3.0mm Post
• 00813110028242: 4.0mm LO Abutment - 3.0mm Post
• 00813110028235: 3.0mm LO Abutment - 3.0mm Post
• 00813110028228: 2.0mm LO Abutment - 3.0mm Post
• 00813110028211: 1.0mm LO Abutment - 3.0mm Post
• 00813110028204: 5.0mm LO Abutment - 2.0mm Post
• 00813110028198: 4.0mm LO Abutment - 2.0mm Post
• 00813110028181: 3.0mm LO Abutment - 2.0mm Post
• 00813110028174: 2.0mm LO Abutment - 2.0mm Post
• 00813110028167: 1.0mm LO Abutment - 2.0mm Post
• 00813110028150: 5.0mm LO Abutment - 2.5mm Post
• 00813110028143: 4.0mm LO Abutment - 2.5mm Post
• 00813110028136: 3.0mm LO Abutment - 2.5mm Post
• 00813110028129: 2.0mm LO Abutment - 2.5mm Post
• 00813110028112: 1.0mm LO Abutment - 2.5mm Post