Multi Temporary Cylinder

GUDID 08809971099844

ARUM DENTISTRY Co., Ltd.

Dental implant suprastructure, permanent, preformed
Primary Device ID08809971099844
NIH Device Record Keybfe00f3b-a0d7-440d-bf07-b238d51701db
Commercial Distribution StatusIn Commercial Distribution
Brand NameMulti Temporary Cylinder
Version Model NumberMTEC55SP
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
GS108809971099844 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08809971099844]

Moist Heat or Steam Sterilization


[08809971099844]

Moist Heat or Steam Sterilization


[08809971099844]

Moist Heat or Steam Sterilization


[08809971099844]

Moist Heat or Steam Sterilization


[08809971099844]

Moist Heat or Steam Sterilization


[08809971099844]

Moist Heat or Steam Sterilization


[08809971099844]

Moist Heat or Steam Sterilization


[08809971099844]

Moist Heat or Steam Sterilization


[08809971099844]

Moist Heat or Steam Sterilization


[08809971099844]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-20
Device Publish Date2026-03-12

On-Brand Devices [Multi Temporary Cylinder]

08809971099998NMTEC55B
08809971099981NMTEC55S
08809971099974MTEC55B
08809971099967MTEC55S
08809971099851MTEC55BP
08809971099844MTEC55SP

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