OMNI Tapered Fixture

GUDID 08800076400429

Truabutment Korea Co.,Ltd

Screw endosteal dental implant, two-piece

• Primary Device ID: 08800076400429
• NIH Device Record Key: a9cb0d82-6540-47bb-97e9-7e4bb0fbcaeb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OMNI Tapered Fixture
• Version Model Number: NTF30115
• Company DUNS: 694514760
• Company Name: Truabutment Korea Co.,Ltd
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800076400429 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K200817

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: 2026-01-29
• Device Publish Date: 2026-01-21

On-Brand Devices [OMNI Tapered Fixture]

• 08800076400795: NTF65100
• 08800076400443: NTF30145
• 08800076400436: NTF30130
• 08800076400429: NTF30115
• 08800076400412: NTF30100