UF(II) Eco Base Abutment

GUDID 08800049430569

DIO Corporation

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08800049430569
• NIH Device Record Key: 756c6cad-6dda-4e01-83cc-e560fa1dd164
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UF(II) Eco Base Abutment
• Version Model Number: USBA 4501H
• 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	08800049430569 [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

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

Moist Heat or Steam Sterilization

[08800049430569]

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 Base Abutment]

• 08800049430958: USBA 6505N
• 08800049430941: USBA 6505H
• 08800049430934: USBA 6504N
• 08800049430927: USBA 6504H
• 08800049430910: USBA 6503N
• 08800049430903: USBA 6503H
• 08800049430897: USBA 6502N
• 08800049430880: USBA 6502H
• 08800049430873: USBA 6501N
• 08800049430866: USBA 6501H
• 08800049430859: USBA 5505N
• 08800049430842: USBA 5505H
• 08800049430835: USBA 5504N
• 08800049430828: USBA 5504H
• 08800049430811: USBA 5503N
• 08800049430804: USBA 5503H
• 08800049430798: USBA 5502N
• 08800049430781: USBA 5502H
• 08800049430774: USBA 5501N
• 08800049430767: USBA 5501H
• 08800049430750: USBA 4805N
• 08800049430743: USBA 4805H
• 08800049430736: USBA 4804N
• 08800049430729: USBA 4804H
• 08800049430712: USBA 4803N
• 08800049430705: USBA 4803H
• 08800049430699: USBA 4802N
• 08800049430682: USBA 4802H
• 08800049430675: USBA 4801N
• 08800049430668: USBA 4801H
• 08800049430651: USBA 4505N
• 08800049430644: USBA 4505H
• 08800049430637: USBA 4504N
• 08800049430620: USBA 4504H
• 08800049430613: USBA 4503N
• 08800049430606: USBA 4503H
• 08800049430590: USBA 4502N
• 08800049430583: USBA 4502H
• 08800049430576: USBA 4501N
• 08800049430569: USBA 4501H