SD TL Fixture

GUDID 08800293192312

ARUM DENTISTRY Co., Ltd.

Screw endosteal dental implant, two-piece
Primary Device ID08800293192312
NIH Device Record Keycb9f6612-b16f-4625-8f4a-9f274256747d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSD TL Fixture
Version Model NumberT5008L
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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800293192312 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-01-19
Device Publish Date2026-01-09

On-Brand Devices [SD TL Fixture]

08800293192084T4511R
08800293192077T4510R
08800293192060T4508R
08800293192053T4507R
08800293192046T4013R
08800293192039T4011R
08800293192022T4010R
08800293192015T4008R
08800293192008T4007R
08800293191995T3613R
08800293191988T3611R
08800293191971T3610R
08800293191964T3608R
08800293191957T3607R
08800293192343T5013L
08800293192336T5011L
08800293192329T5010L
08800293192312T5008L
08800293192305T5007L
08800293192299T4513L
08800293192282T4511L
08800293192275T4510L
08800293192268T4508L
08800293192251T4507L
08800293192244T4013L
08800293192237T4011L
08800293192220T4010L
08800293192213T4008L
08800293192206T4007L
08800293192190T3613L
08800293192183T3611L
08800293192176T3610L
08800293192169T3608L
08800293192152T3607L
08800293192145T5013R
08800293192121T5010R
08800293192114T5008R
08800293192107T5007R
08800293192091T4513R

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