FlexiBuff Regular 5/8

GUDID D7794016581

COSMEDENT, INC.

Dental abrasive disk, single-use

• Primary Device ID: D7794016581
• NIH Device Record Key: 5e819f6e-67c0-4087-92ca-8e79eb456aed
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FlexiBuff Regular 5/8
• Version Model Number: 401658
• Company DUNS: 113911689
• Company Name: COSMEDENT, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7794016581 [Primary]

FDA Product Code

• EHJ: Disk, Abrasive

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: 2020-05-06
• Device Publish Date: 2020-01-22

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• D7796722A31 - Bulkfill: 2022-03-09
• D7796722B11 - Bulkfill: 2022-03-09