ET III Fixture NH Mini D3.2 No Mount

GUDID 00810126044259

HIOSSEN, INC.

Screw endosteal dental implant, two-piece

• Primary Device ID: 00810126044259
• NIH Device Record Key: 99384e86-1470-43ec-a4bc-0a0e125f2c9e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ET III Fixture NH Mini D3.2 No Mount
• Version Model Number: CET3M3011B
• 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	00810126044259 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K151626

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

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: 2025-10-07
• Device Publish Date: 2025-09-29

On-Brand Devices [ET III Fixture NH Mini D3.2 No Mount]

• 00814913028859: CET3M3015B
• 00814913028842: CET3M3013B
• 00814913028835: CET3M3011B
• 00814913028828: CET3M3010B
• 00814913028811: CET3M3008B
• 00810126044297: CET3M3015B
• 00810126044273: CET3M3013B
• 00810126044259: CET3M3011B
• 00810126044235: CET3M3010B
• 00810126044211: CET3M3008B