Porcelize 906105

GUDID D7799061050

COSMEDENT, INC.

Dental abrasive powder Dental abrasive powder

• Primary Device ID: D7799061050
• NIH Device Record Key: 37c9739b-7b1b-4f64-af35-dc0261872f17
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Porcelize
• Version Model Number: 906105
• Catalog Number: 906105
• 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	D7799061050 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K854588

FDA Product Code

• EJR: Agent, Polishing, Abrasive, Oral Cavity

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 [Porcelize]

• D7799061050: 906105
• D7799061040: 906104