Slim Line EUS203014

GUDID 08809691361122

Endosseous dental implant

Dentium Co., Ltd.

Screw endosteal dental implant, two-piece

• Primary Device ID: 08809691361122
• NIH Device Record Key: 7a79ac1c-2330-4fa0-8d5f-ae5b47530ac8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Slim Line
• Version Model Number: EUS203014
• Catalog Number: EUS203014
• Company DUNS: 689514395
• Company Name: Dentium Co., Ltd.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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

Customer Support Contacts

• Phone: +1(714)226-0229
• Email: cs@dentiumusa.com
• Phone: +1(714)226-0229
• Email: cs@dentiumusa.com
• Phone: +1(714)226-0229
• Email: cs@dentiumusa.com
• Phone: +1(714)226-0229
• Email: cs@dentiumusa.com
• Phone: +1(714)226-0229
• Email: cs@dentiumusa.com
• Phone: +1(714)226-0229
• Email: cs@dentiumusa.com
• Phone: +1(714)226-0229
• Email: cs@dentiumusa.com
• Phone: +1(714)226-0229
• Email: cs@dentiumusa.com
• Phone: +1(714)226-0229
• Email: cs@dentiumusa.com

Device Dimensions

• Device Size Text, specify: 0
• Length: 14 Millimeter
• Device Size Text, specify: 0
• Length: 14 Millimeter
• Device Size Text, specify: 0
• Length: 14 Millimeter
• Device Size Text, specify: 0
• Length: 14 Millimeter
• Device Size Text, specify: 0
• Length: 14 Millimeter
• Device Size Text, specify: 0
• Length: 14 Millimeter
• Device Size Text, specify: 0
• Length: 14 Millimeter
• Device Size Text, specify: 0
• Length: 14 Millimeter
• Device Size Text, specify: 0
• Length: 14 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809691361122 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111162

FDA Product Code

• DZE: IMPLANT, ENDOSSEOUS, ROOT-FORM

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-30
• Device Publish Date: 2021-08-20

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