URIS Scan Post Kit Case

GUDID 08800076474932

Truabutment Korea Co.,Ltd

Dental implant kit
Primary Device ID08800076474932
NIH Device Record Keydf476632-bd46-49ea-8cc6-4355c1bee226
Commercial Distribution StatusIn Commercial Distribution
Brand NameURIS Scan Post Kit Case
Version Model NumberUSP-PSBCASE
Company DUNS694514760
Company NameTruabutment Korea 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
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
GS108800076474932 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800076474932]

Moist Heat or Steam Sterilization


[08800076474932]

Moist Heat or Steam Sterilization


[08800076474932]

Moist Heat or Steam Sterilization


[08800076474932]

Moist Heat or Steam Sterilization


[08800076474932]

Moist Heat or Steam Sterilization


[08800076474932]

Moist Heat or Steam Sterilization


[08800076474932]

Moist Heat or Steam Sterilization


[08800076474932]

Moist Heat or Steam Sterilization


[08800076474932]

Moist Heat or Steam Sterilization


[08800076474932]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-04-01
Device Publish Date2026-03-24

On-Brand Devices [URIS Scan Post Kit Case]

08800076474932USP-PSBCASE
08800076464193USP-SBCASE
08800076464186UOM-SBCASE

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.