Temporary Abutment

GUDID 08809982759669

ARUM DENTISTRY Co., Ltd.

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08809982759669
• NIH Device Record Key: cd74f293-b193-478a-a1d0-800374ac68e0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Temporary Abutment
• Version Model Number: LSD401
• Company DUNS: 557821945
• Company Name: ARUM DENTISTRY 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: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809982759669 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K250280

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08809982759669]

Moist Heat or Steam Sterilization

[08809982759669]

Moist Heat or Steam Sterilization

[08809982759669]

Moist Heat or Steam Sterilization

[08809982759669]

Moist Heat or Steam Sterilization

[08809982759669]

Moist Heat or Steam Sterilization

[08809982759669]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-01-19
• Device Publish Date: 2026-01-09

On-Brand Devices [Temporary Abutment]

• 08809982759713: LSD403N
• 08809982759706: LSD401N
• 08809982759690: LSD373MN
• 08809982759683: LSD371MN
• 08809982759676: LSD403
• 08809982759669: LSD401
• 08809982759652: LSD373M
• 08809982759645: LSD371M