ProGlass 17KT01

GUDID 07290016787344

Dental Glass Ionomer

SILMET LTD

Glass ionomer dental cement

• Primary Device ID: 07290016787344
• NIH Device Record Key: 6d24917f-2d36-4b1d-a027-79002652f477
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProGlass
• Version Model Number: 17KT01
• Catalog Number: 17KT01
• Company DUNS: 600071344
• Company Name: SILMET LTD
• 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	07290016787344 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101869

FDA Product Code

• EMA: Cement, Dental

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-12-03
• Device Publish Date: 2017-01-31

On-Brand Devices [ProGlass]

• 07290016787436: Dental Glass Ionomer Cement
• 07290016787429: Dental Glass Ionomer Cement
• 07290016787412: Dental Glass Ionomer Cement
• 07290016787405: Dental Glass Ionomer Cement
• 07290016787399: Dental Glass Ionomer Cement
• 07290016787382: Dental Glass Ionomer Cement
• 07290016787375: Dental Glass Ionomer Cement
• 07290016787368: Dental Glass Ionomer Cement
• 07290016787351: Dental Glass Ionomer Cement
• 07290016787344: Dental Glass Ionomer