EK RIGID ABUTMENT

GUDID 00810019246289

HIOSSEN, INC.

Screw endosteal dental implant, two-piece

• Primary Device ID: 00810019246289
• NIH Device Record Key: f7999c17-41d3-476c-941a-4882dd9d47ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EK RIGID ABUTMENT
• Version Model Number: EKRA6740P
• 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: 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	00810019246289 [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

Devices Manufactured by HIOSSEN, INC.

• 00810126040008 - EK III NH Fixture Pre-Mounted: 2024-09-26
• 00810126040015 - EK III NH Fixture Pre-Mounted: 2024-09-26
• 00810126040022 - EK III NH Fixture Pre-Mounted: 2024-09-26
• 00810126040039 - EK III NH Fixture Pre-Mounted: 2024-09-26
• 00810126040046 - EK III NH Fixture Pre-Mounted: 2024-09-26
• 00810126040053 - EK III NH Fixture Pre-Mounted: 2024-09-26
• 00810126040060 - EK III NH Fixture Pre-Mounted: 2024-09-26
• 00810126040077 - EK III NH Fixture Pre-Mounted: 2024-09-26