Myerson MO

GUDID 00842326146365

MO Posterior shade DK, U

The Myerson Company Limited

Resin artificial teeth

• Primary Device ID: 00842326146365
• NIH Device Record Key: df89ac4f-2320-43ac-b043-935b5a4c58dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Myerson MO
• Version Model Number: TMDKU
• Company DUNS: 857278431
• Company Name: The Myerson Company Limited
• 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: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 18004232683
• Email: orders@myersontooth.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842326146365 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K924526

FDA Product Code

• ELM: Denture, Plastic, Teeth

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: 2016-09-24

On-Brand Devices [Myerson MO]

• 00842326146402: MO Posterior shade MD, U
• 00842326146396: MO Posterior shade MD, L
• 00842326146389: MO Posterior shade LT, U
• 00842326146372: MO Posterior shade LT, L
• 00842326146365: MO Posterior shade DK, U
• 00842326146358: MO Posterior shade DK, L