Coping 260-105-700

GUDID 00813110027528

UA5 LP Retentive Copings (2)

BICON, LLC

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 00813110027528
• NIH Device Record Key: 158fe852-30f2-4679-9337-1570e8af8593
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Coping
• Version Model Number: 260-105-700
• Catalog Number: 260-105-700
• 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	00813110027528 [Primary]
GS1	00813110027634 [Unit of Use]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[00813110027528]

Moist Heat or Steam Sterilization

[00813110027528]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-03-25
• Device Publish Date: 2016-09-19

On-Brand Devices [Coping]

• 00813110027559: UA5 SP/TP Passive Copings (2)
• 00813110027542: UA5 SP/TP Retentive Copings (2)
• 00813110027535: UA5 LP Passive Copings (2)
• 00813110027528: UA5 LP Retentive Copings (2)
• 00813110029522: UA5 SP/TP Retentive Ring (2)
• 00813110029515: UA5 LP Retentive Ring (2)