Trial Pin

GUDID 08800055792958

ARUM DENTISTRY Co., Ltd.

Dental implantation depth/angle gauge, reusable
Primary Device ID08800055792958
NIH Device Record Key1cc66e39-2e05-477c-8b85-9e641b0fd919
Commercial Distribution StatusIn Commercial Distribution
Brand NameTrial Pin
Version Model NumberTP5513
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
GS108800055792958 [Primary]

FDA Product Code

NDPAccessories, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800055792958]

Moist Heat or Steam Sterilization


[08800055792958]

Moist Heat or Steam Sterilization


[08800055792958]

Moist Heat or Steam Sterilization


[08800055792958]

Moist Heat or Steam Sterilization


[08800055792958]

Moist Heat or Steam Sterilization


[08800055792958]

Moist Heat or Steam Sterilization


[08800055792958]

Moist Heat or Steam Sterilization


[08800055792958]

Moist Heat or Steam Sterilization


[08800055792958]

Moist Heat or Steam Sterilization


[08800055792958]

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 [Trial Pin]

08800055792972TP6513
08800055792965TP6013
08800055792958TP5513

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