Direct Clip Abutment

GUDID 00810008462010

THE TONY FECK™ Direct Clip Abutment - ht 5

Little Implant Co.

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 00810008462010
• NIH Device Record Key: 0bcf27aa-a54a-4f10-acd3-fd0cbc903534
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Direct Clip Abutment
• Version Model Number: RRDCA5
• 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: false
• 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	00810008462010 [Primary]

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[00810008462010]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-08
• Device Publish Date: 2019-05-13

On-Brand Devices [Direct Clip Abutment]

• 00810008462010: THE TONY FECK™ Direct Clip Abutment - ht 5
• 00810008462003: THE TONY FECK™ Direct Clip Abutment - ht 3
• 00810008461990: THE TONY FECK™ Direct Clip Abutments-ht 1