Digital Anchor Kit

GUDID 08800293195078

ARUM DENTISTRY Co., Ltd.

Dental/maxillofacial surgical procedure kit, non-medicated, reusable
Primary Device ID08800293195078
NIH Device Record Keye54bbb32-fc02-484d-a975-e7e27220b99b
Commercial Distribution StatusIn Commercial Distribution
Brand NameDigital Anchor Kit
Version Model NumberDIAK-SET
Company DUNS557821945
Company NameARUM DENTISTRY Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
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
GS108800293195078 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800293195078]

Moist Heat or Steam Sterilization

[08800293195078]

Moist Heat or Steam Sterilization

[08800293195078]

Moist Heat or Steam Sterilization

[08800293195078]

Moist Heat or Steam Sterilization

[08800293195078]

Moist Heat or Steam Sterilization

[08800293195078]

Moist Heat or Steam Sterilization

[08800293195078]

Moist Heat or Steam Sterilization

[08800293195078]

Moist Heat or Steam Sterilization

[08800293195078]

Moist Heat or Steam Sterilization

[08800293195078]

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

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08800055792910 - Torque Extension2026-04-01
08800055792958 - Trial Pin2026-04-01
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