Tilite Chrome Discs

GUDID D791252250

TALLADIUM, INC.

Dental casting non-noble alloy

• Primary Device ID: D791252250
• NIH Device Record Key: 30617a28-02b4-4027-b288-a6da3d409003
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tilite Chrome Discs
• Version Model Number: 25225
• Company DUNS: 094430642
• Company Name: TALLADIUM, 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: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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
HIBCC	D791252250 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K894085

FDA Product Code

• EJH: Alloy, Metal, Base

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-11-10

On-Brand Devices [Tilite Chrome Discs]

• D791252280: 25228
• D791252270: 25227
• D791252260: 25226
• D791252250: 25225
• D791252240: 25224
• D791252230: 25223
• D791252220: 25222