HG III Fixture Mini RBM No Mount

GUDID 00814913022222

HIOSSEN, INC.

Screw endosteal dental implant, two-piece

• Primary Device ID: 00814913022222
• NIH Device Record Key: 5413f3dc-14ff-46db-aa3e-0207061819dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HG III Fixture Mini RBM No Mount
• Version Model Number: CHG3M3515R
• 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	00814913022222 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082213

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-02

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