Temporary Cylinder

GUDID 08800049416884

DIO Corporation

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08800049416884
• NIH Device Record Key: da622b28-e6a5-4300-9337-a9f5bcba38f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Temporary Cylinder
• Version Model Number: ITC 48010
• Company DUNS: 631085206
• Company Name: DIO Corporation
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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	08800049416884 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122519

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08800049416884]

Moist Heat or Steam Sterilization

[08800049416884]

Moist Heat or Steam Sterilization

[08800049416884]

Moist Heat or Steam Sterilization

[08800049416884]

Moist Heat or Steam Sterilization

[08800049416884]

Moist Heat or Steam Sterilization

[08800049416884]

Moist Heat or Steam Sterilization

[08800049416884]

Moist Heat or Steam Sterilization

[08800049416884]

Moist Heat or Steam Sterilization

[08800049416884]

Moist Heat or Steam Sterilization

[08800049416884]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-29
• Device Publish Date: 2025-09-19

On-Brand Devices [Temporary Cylinder]

• 08800049251423: MTEM 5412N
• 08800049251416: MTEM 5412H
• 08800049416884: ITC 48010