CONTOUR ABUTMENT SPLINE 4350 TSI-ERI (SPLINE)

GUDID D7854350TSIERISP0

NATURAL CONTOUR ESTHETIC ABUTMENT (SPLINE)

OCO BIOMEDICAL INC

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: D7854350TSIERISP0
• NIH Device Record Key: cbb27790-904d-440d-a80d-fb5a8b3585a2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CONTOUR ABUTMENT SPLINE
• Version Model Number: NATURAL CONTOUR ESTHETIC ABUTMENT SPLINE
• Catalog Number: 4350 TSI-ERI (SPLINE)
• Company DUNS: 094146123
• Company Name: OCO BIOMEDICAL INC
• Device Count: 1
• DM Exempt: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7854350TSIERISP0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090174

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

[D7854350TSIERISP0]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-02-22
• Device Publish Date: 2024-02-14

On-Brand Devices [CONTOUR ABUTMENT SPLINE]

• D7855350TSIERISP0: NATURAL CONTOUR ESTHETIC ABUTMENT (SPLINE)
• D7854350TSIERISP0: NATURAL CONTOUR ESTHETIC ABUTMENT (SPLINE)