Multi Scan Healing Cap Screw

GUDID 08800265647017

ARUM DENTISTRY Co., Ltd.

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 08800265647017
• NIH Device Record Key: 87886bc7-8d42-46b0-ad6a-c2b198fd83d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multi Scan Healing Cap Screw
• Version Model Number: MSHS35
• Company DUNS: 557821945
• Company Name: ARUM DENTISTRY Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800265647017 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241703

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: 2026-03-20
• Device Publish Date: 2026-03-12

On-Brand Devices [Multi Scan Healing Cap Screw]

• 08800265647048: NMSHS50
• 08800265647031: NMSHS35
• 08800265647024: NMSHS35
• 08800265647017: MSHS35