MOR® RC-2

GUDID 00841549115721

10 pack. A female part which is inserted into the acrylic overdenture and houses changeable nylon retention inserts.

STERNGOLD DENTAL LLC

Resilient dental precision attachment

• Primary Device ID: 00841549115721
• NIH Device Record Key: 640a32c9-4f89-4683-b464-ebe68241ad34
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MOR® RC-2
• Version Model Number: 904815
• Company DUNS: 124763728
• Company Name: STERNGOLD DENTAL LLC
• 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: 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

Customer Support Contacts

• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com
• Phone: 5082265660
• Email: laura.greige@sterngold.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841549115721 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153173

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

[00841549115721]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-13
• Device Publish Date: 2023-10-05

On-Brand Devices [MOR® RC-2 ]

• 00841549113659: A female part which is inserted into the acrylic overdenture and houses changeable nylon retenti
• 00841549115721: 10 pack. A female part which is inserted into the acrylic overdenture and houses changeable nyl