Titanium Non-Engaging Temporary Abutment 6035-49

GUDID 10841307113980

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 10841307113980
• NIH Device Record Key: a7adad11-dda4-45d6-be61-b5961c88ccbb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Titanium Non-Engaging Temporary Abutment
• Version Model Number: 6035-49
• Catalog Number: 6035-49
• Company DUNS: 868856969
• Company Name: IMPLANT DIRECT SYBRON MANUFACTURING 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: 1-888-649-6425
• Email: customerservice@implantdirect.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841307113980 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081101

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[10841307113980]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-08
• Device Publish Date: 2015-09-14

On-Brand Devices [Titanium Non-Engaging Temporary Abutment]

• 10841307115472: 2065-49
• 10841307115274: 1057-49
• 10841307115267: 1047-49
• 10841307115250: 1037-49
• 10841307114017: 6060-49
• 10841307114000: 6050-49
• 10841307113997: 6043-49
• 10841307113980: 6035-49