THE TONY FECK™

GUDID 00810008462904

THE TONY FECK™ Internal Hex Implant 3.0 dia. x L10mm

Little Implant Co.

Screw endosteal dental implant, one-piece

• Primary Device ID: 00810008462904
• NIH Device Record Key: fe77ca52-0249-44ab-b516-9d25ea5cb156
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: THE TONY FECK™
• Version Model Number: RR3010
• Company DUNS: 050003777
• Company Name: Little Implant Co.
• Device Count: 1
• DM Exempt: true
• 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: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810008462904 [Primary]

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: 2019-05-21
• Device Publish Date: 2019-05-13

On-Brand Devices [THE TONY FECK™]

• 00810008462928: THE TONY FECK™ Internal Hex Implant 3.0 dia. x L14mm
• 00810008462911: THE TONY FECK™ Internal Hex Implant 3.0 dia. x L12mm
• 00810008462904: THE TONY FECK™ Internal Hex Implant 3.0 dia. x L10mm
• 00810008462898: THE TONY FECK™ Internal Hex Implant 3.0 dia. x L8mm