Closing Screw

GUDID 08800039364652

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

Dental implant system

• Primary Device ID: 08800039364652
• NIH Device Record Key: a7f333a0-9b0a-4a54-9da1-49ce5609cd62
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Closing Screw
• Version Model Number: HISCS
• 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: 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	08800039364652 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220517

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-09-01
• Device Publish Date: 2023-01-03

On-Brand Devices [Closing Screw]

• 08800039315364: HISCY
• 08800039364652: HISCS