Magic FC

GUDID 08800039380706

InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)

Dental implant system

• Primary Device ID: 08800039380706
• NIH Device Record Key: 094f6e0d-11a5-43c2-9026-9192282b50ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Magic FC
• Version Model Number: IBS5013FC
• Company DUNS: 631169224
• Company Name: InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800039380706 [Primary]

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-08-25
• Device Publish Date: 2020-08-17

On-Brand Devices [Magic FC]

• 08800039380591: IBS4007FC
• 08800039380829: IBS6513FC
• 08800039380812: IBS6511FC
• 08800039380805: IBS6509FC
• 08800039380782: IBS6013FC
• 08800039380775: IBS6011FC
• 08800039380768: IBS6009FC
• 08800039380751: IBS6007FC
• 08800039380744: IBS5513FC
• 08800039380737: IBS5511FC
• 08800039380720: IBS5509FC
• 08800039380713: IBS5507FC
• 08800039380706: IBS5013FC
• 08800039380690: IBS5011FC
• 08800039380683: IBS5009FC
• 08800039380676: IBS5007FC
• 08800039380669: IBS4513FC
• 08800039380652: IBS4511FC
• 08800039380645: IBS4509FC
• 08800039380638: IBS4507FC
• 08800039380621: IBS4013FC
• 08800039380614: IBS4011FC
• 08800039380607: IBS4009FC