CLEARFIL MAJESTY™ ES Flow

GUDID EKUR003308KA1

B2

KURARAY NORITAKE DENTAL INC.

Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin

• Primary Device ID: EKUR003308KA1
• NIH Device Record Key: 7b12dd29-d786-4f85-b4ad-171ef5466897
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLEARFIL MAJESTY™ ES Flow
• Version Model Number: #3308-KA
• Company DUNS: 697119498
• Company Name: KURARAY NORITAKE DENTAL 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	EKUR003308KA1 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130371
• Premarket Notification: K191980

FDA Product Code

• EBF: Material, Tooth Shade, 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: 2018-07-06
• Device Publish Date: 2017-02-17

On-Brand Devices [CLEARFIL MAJESTY™ ES Flow]

• EKUR003331KA1: Needle tip (N)
• EKUR003317KA1: TRIAL (A2)
• EKUR003312KA1: W
• EKUR003309KA1: XW
• EKUR003308KA1: B2
• EKUR003307KA1: B1
• EKUR003306KA1: KA6
• EKUR003305KA1: A4
• EKUR003304KA1: A3.5
• EKUR003303KA1: A3
• EKUR003302KA1: A2
• EKUR003301KA1: A1