Vivid SoloTemp

GUDID D724N1104620

A1

PEARSON DENTAL SUPPLIES, INC.

Temporary dental crown/bridge resin

• Primary Device ID: D724N1104620
• NIH Device Record Key: dc3340fe-bc10-42d2-8941-3f411b15ed91
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vivid SoloTemp
• Version Model Number: N110462
• Company DUNS: 082874108
• Company Name: PEARSON DENTAL SUPPLIES, 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: true
• 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	D724N1104620 [Primary]

FDA Product Code

• EBG: Crown And Bridge, Temporary, Resin

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: 2021-10-29
• Device Publish Date: 2016-06-09

On-Brand Devices [Vivid SoloTemp]

• D724N1104690: C2
• D724N1104680: A3
• D724N1104660: B1
• D724N1104640: A2
• D724N1104620: A1
• D724N1104600: BL