EK ANGLED ABUTMENT(N)

GUDID 00810019248726

HIOSSEN, INC.

Screw endosteal dental implant, two-piece

• Primary Device ID: 00810019248726
• NIH Device Record Key: 560e1d96-3c87-46a2-87e9-8e7236f3bb12
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EK ANGLED ABUTMENT(N)
• Version Model Number: EKAA5020NTH
• 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	00810019248726 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K203360

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: 2022-05-31
• Device Publish Date: 2022-05-23

On-Brand Devices [EK ANGLED ABUTMENT(N)]

• 00810019248818: EKAA6040NTH
• 00810019248788: EKAA6020NTH
• 00810019248757: EKAA5040NTH
• 00810019248726: EKAA5020NTH
• 00810019248696: EKAA4540NTH
• 00810019248665: EKAA4520NTH
• 00810019248634: EKAA4040NTH
• 00810019248603: EKAA4020NTH