Retaining Screw

GUDID 08800039379618

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

Dental implant system

• Primary Device ID: 08800039379618
• NIH Device Record Key: b0a32c72-2255-4d50-a897-bde0a37aa86c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Retaining Screw
• Version Model Number: MASR
• 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: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: true
• 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	08800039379618 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173120

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

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: 2024-10-23
• Device Publish Date: 2024-10-15

Devices Manufactured by InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd)

• 08800039381857 - Magic Depth Drill: 2025-09-03
• 08800039381871 - Magic Depth Drill: 2025-09-03
• 08800039381888 - Magic Depth Drill: 2025-09-03
• 08800177332582 - Magicore S: 2025-09-03
• 08800039307802 - Guide Drill: 2025-09-01
• 08800039307819 - Magic Depth Drill: 2025-09-01
• 08800039307826 - Magic Depth Drill: 2025-09-01
• 08800039307864 - Guide Drill: 2025-09-01