ATLANTIS®

GUDID 07392532291586

ATLANTIS Conus Abutment Cu Gold Duplicate

DENTSPLY IH, INC.

Transgingival implant

• Primary Device ID: 07392532291586
• NIH Device Record Key: e5c66138-928e-4bd5-8ba5-e58825a54b48
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ATLANTIS®
• Version Model Number: 35355
• Company DUNS: 847337201
• Company Name: DENTSPLY IH, INC.
• Device Count: 1
• DM Exempt: false
• 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: false
• Manufacturing Date: true
• 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

Customer Support Contacts

• Phone: +1(800)531-3481
• Email: implants-na-cs@dentsply.com
• Phone: +1(800)531-3481
• Email: implants-na-cs@dentsply.com
• Phone: +1(800)531-3481
• Email: implants-na-cs@dentsply.com
• Phone: +1(800)531-3481
• Email: implants-na-cs@dentsply.com
• Phone: +1(800)531-3481
• Email: implants-na-cs@dentsply.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Storage in the original packaging, in a dry place, at normal room temperature.
• Special Storage Condition, Specify: Between 0 and 0 *Storage in the original packaging, in a dry place, at normal room temperature.
• Special Storage Condition, Specify: Between 0 and 0 *Storage in the original packaging, in a dry place, at normal room temperature.
• Special Storage Condition, Specify: Between 0 and 0 *Storage in the original packaging, in a dry place, at normal room temperature.
• Special Storage Condition, Specify: Between 0 and 0 *Storage in the original packaging, in a dry place, at normal room temperature.

Device Identifiers

Device Issuing Agency	Device ID
GS1	07392532177163 [Previous]
GS1	07392532291586 [Primary]

FDA Product Code

• NHA: Abutment, implant, dental, endosseous

Sterilization

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

[07392532291586]

Moist Heat or Steam Sterilization

[07392532291586]

Moist Heat or Steam Sterilization

[07392532291586]

Moist Heat or Steam Sterilization

[07392532291586]

Moist Heat or Steam Sterilization

[07392532291586]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-23
• Device Publish Date: 2025-12-15

On-Brand Devices [ATLANTIS®]

• 07392532198854: Atlantis Conus Bridge Ti
• 07392532198847: Atlantis Conus Hybrid Ti
• 07392532198830: Atlantis Conus Base Ti
• 07392532198564: Atlantis Temp Crown
• 07392532177095: Atlantis® Insertion Guide
• 07392532213144: Atlantis Healing Abutment GS
• 07392532291661: ATLANTIS Healing Abutment Ti
• 07392532291647: ATLANTIS Abutment Ti Duplicate
• 07392532291616: ATLANTIS Abutment Ti
• 07392532291593: ATLANTIS Crown Abutment Ti
• 07392532291586: ATLANTIS Conus Abutment Cu Gold Duplicate
• 07392532291579: ATLANTIS Conus Abutment Cu Ti Duplicate
• 07392532291555: ATLANTIS Conus Abutment Custom Ti
• 07392532291531: ATLANTIS Conus Abutment OD Ti
• 07392532291524: ATLANTIS Abutment Screw