INTERFACE

GUDID 00850015110443

DENTAL CAVITY LINER DENTIN SHADE

TEMREX CORPORATION

Dental acrylic resin

• Primary Device ID: 00850015110443
• NIH Device Record Key: 87b93f55-693c-462f-98de-1bcfa9811c8b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INTERFACE
• Version Model Number: 7110
• Company DUNS: 012072823
• Company Name: TEMREX CORPORATION
• 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: false
• Manufacturing Date: false
• 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	00850015110443 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K897130

FDA Product Code

• EJK: Liner, Cavity, Calcium Hydroxide

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: 2020-02-20
• Device Publish Date: 2020-02-12

On-Brand Devices [INTERFACE]

• 00850015110443: DENTAL CAVITY LINER DENTIN SHADE
• 00850015110436: DENTAL CAVITY LINER DENTIN SHADE