HG III Ultra-Wide Fixture RBM Pre-Mounted

GUDID 00814913022147

HIOSSEN, INC.

Screw endosteal dental implant, two-piece Screw endosteal dental implant, two-piece

• Primary Device ID: 00814913022147
• NIH Device Record Key: aa7715b6-25fc-4a86-894e-52f7207e176f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HG III Ultra-Wide Fixture RBM Pre-Mounted
• Version Model Number: AHG3S7008R
• 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	00814913022147 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093889

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

On-Brand Devices [HG III Ultra-Wide Fixture RBM Pre-Mounted]

• 00814913022178: AHG3S7013R
• 00814913022161: AHG3S7011R
• 00814913022154: AHG3S7010R
• 00814913022147: AHG3S7008R
• 00814913022130: AHG3S7007R
• 00814913022123: AHG3S6013R
• 00814913022116: AHG3S6011R
• 00814913022109: AHG3S6010R
• 00814913022093: AHG3S6008R
• 00814913022086: AHG3S6007R