RITON

GUDID 06975902950132

Riton 3D Technology Co., Ltd

Dental appliance fabrication material, resin
Primary Device ID06975902950132
NIH Device Record Key095883e1-c5db-41f3-94e1-b9e675bf00b6
Commercial Distribution StatusIn Commercial Distribution
Brand NameRITON
Version Model NumberS1.0
Company DUNS842156344
Company NameRiton 3D Technology Co., Ltd
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106975902950132 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-06-17
Device Publish Date2024-06-07

On-Brand Devices [RITON]

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

Trademark Results [RITON]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RITON
RITON
86021966 5059830 Live/Registered
Riton America, LLC
2013-07-29

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