URIS Scan Post

GUDID 08800076423664

Truabutment Korea Co.,Ltd

Dental implant abutment analog, intraoral-scanning, single-use
Primary Device ID08800076423664
NIH Device Record Keye07400aa-b77c-43aa-aea4-41bd32e13b04
Commercial Distribution StatusIn Commercial Distribution
Brand NameURIS Scan Post
Version Model NumberUSPN4018
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
GS108800076423664 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800076423664]

Moist Heat or Steam Sterilization


[08800076423664]

Moist Heat or Steam Sterilization


[08800076423664]

Moist Heat or Steam Sterilization


[08800076423664]

Moist Heat or Steam Sterilization


[08800076423664]

Moist Heat or Steam Sterilization


[08800076423664]

Moist Heat or Steam Sterilization


[08800076423664]

Moist Heat or Steam Sterilization


[08800076423664]

Moist Heat or Steam Sterilization


[08800076423664]

Moist Heat or Steam Sterilization


[08800076423664]

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]

08800076423725USPR4538
08800076423718USPR4528
08800076423701USPR4518
08800076423695USPR4508
08800076423688USPN4038
08800076423671USPN4028
08800076423664USPN4018

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