Multi Master Fix Screw

GUDID 08800265645389

ARUM DENTISTRY Co., Ltd.

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08800265645389
• NIH Device Record Key: eb2822d9-c01f-427b-bd58-f10f0c4fd91b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multi Master Fix Screw
• Version Model Number: MMFS25T
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800265645389 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241703

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08800265645389]

Moist Heat or Steam Sterilization

[08800265645389]

Moist Heat or Steam Sterilization

[08800265645389]

Moist Heat or Steam Sterilization

[08800265645389]

Moist Heat or Steam Sterilization

[08800265645389]

Moist Heat or Steam Sterilization

[08800265645389]

Moist Heat or Steam Sterilization

[08800265645389]

Moist Heat or Steam Sterilization

[08800265645389]

Moist Heat or Steam Sterilization

[08800265645389]

Moist Heat or Steam Sterilization

[08800265645389]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-20
• Device Publish Date: 2026-03-12

On-Brand Devices [Multi Master Fix Screw]

• 08800265645396: MMFS35T
• 08800265645389: MMFS25T
• 08800265645372: MMFS15T