Abutment Screw

GUDID 08800055721392

ARUM DENTISTRY Co., Ltd.

Dental implant suprastructure, permanent, preformed
Primary Device ID08800055721392
NIH Device Record Key0aa7d734-1b6f-4557-9266-475a718430fa
Commercial Distribution StatusIn Commercial Distribution
Brand NameAbutment Screw
Version Model NumberCSTO602
Company DUNS557821945
Company NameARUM DENTISTRY Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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
GS108800055721392 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


[08800055721392]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-01-15
Device Publish Date2026-01-07

On-Brand Devices [Abutment Screw]

08809917602268NBMAS
08800055796406NBAS
08800055721392CSTO602
08800055721385CSTO601
08800055717791CSHE016

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