da Vinci 6120W1

GUDID D7796120W10

COSMEDENT, INC.

Fatty acid dental cement

• Primary Device ID: D7796120W10
• NIH Device Record Key: 01ef5aef-7c49-4691-96d5-621dbde4f74f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: da Vinci
• Version Model Number: 6120W1
• Catalog Number: 6120W1
• Company DUNS: 113911689
• Company Name: COSMEDENT, INC.
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7796120W10 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K873356

FDA Product Code

• EMA: Cement, Dental

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-22

On-Brand Devices [da Vinci]

• D7797120W40: 7120W4
• D7797120W30: 7120W3
• D7797120W20: 7120W2
• D7797120W10: 7120W1
• D7797120CL0: 7120CL
• D7796120W40: 6120W4
• D7796120W30: 6120W3
• D7796120W20: 6120W2
• D7796120W10: 6120W1
• D7796120CL0: 6120CL