VITA Akzent Plus

GUDID J017BAPKGS0

VITA AKZENT® Plus GLAZE SAMPLE KIT

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

Dental appliance fabrication material, ceramic

• Primary Device ID: J017BAPKGS0
• NIH Device Record Key: 4606ddab-a7ed-46cb-9dd4-e8c44ea8fbd1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VITA Akzent Plus
• Version Model Number: BAPKGS
• 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: true
• 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
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	J017BAPKGS0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K901982

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: 2021-04-27
• Device Publish Date: 2021-04-19

On-Brand Devices [VITA Akzent Plus]

• J017BAPKGS0: VITA AKZENT® Plus GLAZE SAMPLE KIT
• J017BAPKGLTS0: VITA AKZENT® Plus GLAZE LT SAMPLE KIT
• J017BAPKCSC0: VITA AKZENT® Plus CHROMA STAINS KIT
• J017BAPKV10: VITA AKZENT® Plus POWDER KIT
• J017BAPKSKV10: VITA AKZENT® PLUS MINI KIT
• J017BAPKPV10: VITA AKZENT® Plus PASTE KIT