Korticale TPR IH BITP3512IH

GUDID D169BPIH3512

QUICKDENT DEVICES PRIVATE LIMITED

Dental implant system
Primary Device IDD169BPIH3512
NIH Device Record Keyc036d9d5-c3ff-46e3-a30e-7e137c0a7927
Commercial Distribution StatusIn Commercial Distribution
Brand NameKorticale TPR IH
Version Model Number3.5 x 12mm
Catalog NumberBITP3512IH
Company DUNS860405444
Company NameQUICKDENT DEVICES PRIVATE LIMITED
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD169BPIH3512 [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 Date2025-07-09
Device Publish Date2025-07-01

On-Brand Devices [Korticale TPR IH]

D169BPIH42164.2 x 16mm
D169BPIH42144.2 x 14mm
D169BPIH42124.2 x 12mm
D169BPIH42104.2 x 10mm
D169BPIH35163.5 x 16mm
D169BPIH35143.5 x 14mm
D169BPIH35123.5 x 12mm
D169BPIH35103.5 x 10mm

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