RITON

GUDID 06975902950132

Riton 3D Technology Co., Ltd

Dental appliance fabrication material, resin

• Primary Device ID: 06975902950132
• NIH Device Record Key: 095883e1-c5db-41f3-94e1-b9e675bf00b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RITON
• Version Model Number: S1.0
• Company DUNS: 842156344
• Company Name: Riton 3D Technology Co., Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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
GS1	06975902950132 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

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: 2024-06-17
• Device Publish Date: 2024-06-07

On-Brand Devices [RITON]

• 06975902950026: RXT-01
• 06975902950132: S1.0
• 06975902950118: V3.0