ET Pre-milled Abutment

GUDID 00810126040893

HIOSSEN, INC.

Screw endosteal dental implant, two-piece

• Primary Device ID: 00810126040893
• NIH Device Record Key: 487b39b3-aadc-4b06-a849-9fb8b0f139cd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ET Pre-milled Abutment
• Version Model Number: ETPMA10UKMNW
• 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	00810126040893 [Primary]

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: 2025-02-25
• Device Publish Date: 2025-02-17

On-Brand Devices [ ET Pre-milled Abutment]

• 00810126041111: ETPMA14CARNW
• 00810126040930: ETPMA10ZKMNW
• 00810126040893: ETPMA10UKMNW
• 00810126040879: ETPMA10MXRNW
• 00810126040763: ETPMA10CAMHW