EK 30° Multi Angled abutment

GUDID 00810125998669

HIOSSEN, INC.

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 00810125998669
• NIH Device Record Key: 74c6a985-0fd8-4af5-b4b8-aa4d1a8f743f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EK 30° Multi Angled abutment
• Version Model Number: EK30MA4830TH
• Company DUNS: 796083090
• Company Name: HIOSSEN, INC.
• Device Count: 1
• DM Exempt: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810125998669 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K251427

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-02-12
• Device Publish Date: 2026-02-04

On-Brand Devices [ EK 30° Multi Angled abutment ]

• 00810125998683: EK30MA4850TH
• 00810125998676: EK30MA4840TH
• 00810125998669: EK30MA4830TH