UF(II) Eco Angled Post

GUDID 08800049431924

DIO Corporation

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08800049431924
• NIH Device Record Key: cb1c2b1f-62f2-4abe-8b2e-542d36fa1d72
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UF(II) Eco Angled Post
• Version Model Number: USAP 480806BH
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com
• Phone: 213-365-2875
• Email: usahq@dioimplantusa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800049431924 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220253

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

[08800049431924]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-11
• Device Publish Date: 2023-09-01

On-Brand Devices [UF(II) Eco Angled Post]

• 08800049442722: USAP 450818BH
• 08800049442715: USAP 450818AH
• 08800049442692: USAP 450812BH
• 08800049442685: USAP 450812AH
• 08800049442661: USAP 450806BH
• 08800049442654: USAP 450806AH
• 08800049432068: USAP 550818AH
• 08800049432037: USAP 550812AH
• 08800049432006: USAP 550806AH
• 08800049431979: USAP 480818AH
• 08800049431948: USAP 480812AH
• 08800049431924: USAP 480806BH
• 08800049431917: USAP 480806AH