VITA STARTER KIT

GUDID J017EC4STKITS40

VITA STARTER KIT CAD/CAM BLOCKS (IV)

Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft

Dental appliance fabrication material, ceramic

• Primary Device ID: J017EC4STKITS40
• NIH Device Record Key: 6c27f325-7a83-4090-8433-42881fe26ea2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VITA STARTER KIT
• Version Model Number: VITA STARTER KIT CAD/CAM BLOCKS (IV)
• Company DUNS: 315165357
• Company Name: Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft
• 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: true
• Device Combination Product: false
• Single Use: false
• 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: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	J017EC4STKITS40 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102128

FDA Product Code

• EIH: POWDER, PORCELAIN

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-28
• Device Publish Date: 2024-06-20

Devices Manufactured by Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft

• J017A60M120EO0 - VITA PHYSIODENS®: 2025-07-25 VITA PHYSIODENS Posteriores, 0M1, 20E OK
• J017A60M120EU0 - VITA PHYSIODENS®: 2025-07-25 VITA PHYSIODENS Posteriores, 0M1, 20E UK
• J017A60M121EO0 - VITA PHYSIODENS®: 2025-07-25 VITA PHYSIODENS Posteriores, 0M1, 21E OK
• J017A60M121EU0 - VITA PHYSIODENS®: 2025-07-25 VITA PHYSIODENS Posteriores, 0M1, 21E UK
• J017A60M122EO0 - VITA PHYSIODENS®: 2025-07-25 VITA PHYSIODENS Posteriores, 0M1, 22E OK
• J017A60M122EU0 - VITA PHYSIODENS®: 2025-07-25 VITA PHYSIODENS Posteriores, 0M1, 22E UK
• J017A60M123EO0 - VITA PHYSIODENS®: 2025-07-25 VITA PHYSIODENS Posteriores, 0M1, 23E OK
• J017A60M123EU0 - VITA PHYSIODENS®: 2025-07-25 VITA PHYSIODENS Posteriores, 0M1, 23E UK