AuraOpaquer AOP

GUDID D820AOP0

Opaquer, Dental.

DENALI CORPORATION

Dental composite resin

• Primary Device ID: D820AOP0
• NIH Device Record Key: 0a8e5977-a222-47b1-b77b-969191332992
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AuraOpaquer
• Version Model Number: 1.2 mL Pink
• Catalog Number: AOP
• Company DUNS: 191036107
• Company Name: DENALI CORPORATION
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1-781-826-9190
• Email: denalicorp@denalicorporation.com
• Phone: +1-781-826-9190
• Email: denalicorp@denalicorporation.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D820AOP0 [Primary]
HIBCC	D820AOP1 [Package]; Package: [2 Units]; In Commercial Distribution

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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-05

On-Brand Devices [AuraOpaquer]

• D820AOW1: Opaquer, Dental.
• D820AOP0: Opaquer, Dental.