ET Multi Angled Abutment

GUDID 00810125999116

HIOSSEN, INC.

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• Primary Device ID: 00810125999116
• NIH Device Record Key: 7e0b7d77-2132-4bfe-9598-795984de5d26
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ET Multi Angled Abutment
• Version Model Number: ETMA517SHW
• 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	00810125999116 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K233194

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: 2024-05-15
• Device Publish Date: 2024-05-07

On-Brand Devices [ET Multi Angled Abutment]

• 00814913028750: ETMA530SHW
• 00814913028743: ETMA430SHW
• 00814913028736: ETMA330SHW
• 00814913028729: ETMA417SHW
• 00814913028712: ETMA317SHW
• 00814913028705: ETMA217SHW
• 00814913028699: ETMA530MHW
• 00814913028682: ETMA430MHW
• 00814913028675: ETMA330MHW
• 00814913028668: ETMA417MHW
• 00814913028651: ETMA317MHW
• 00814913028644: ETMA217MHW
• 00810125999116: ETMA517SHW