Magic Motion Abutment

GUDID 08800039321594

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

Dental implant system

• Primary Device ID: 08800039321594
• NIH Device Record Key: 328b0e67-7330-405a-a127-9b89fd1deb3c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Magic Motion Abutment
• Version Model Number: M3512
• 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: 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
GS1	08800039321594 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153350

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2026-03-16
• Device Publish Date: 2018-11-29

On-Brand Devices [Magic Motion Abutment ]

• 08809986680129: M3412
• 08809986680112: M3312
• 08809986680105: M3212
• 08809986680099: M3112
• 08800039321594: M3512
• 08800039321587: M3412
• 08800039321570: M3312
• 08800039321563: M3212