LO 260-300-501

GUDID 00813110028211

1.0mm LO Abutment - 3.0mm Post

BICON, LLC

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 00813110028211
• NIH Device Record Key: 0243fed9-9e75-458c-be03-22bc9e09cdc4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LO
• Version Model Number: 260-300-501
• Catalog Number: 260-300-501
• 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	00813110028211 [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