TRI TRI-11.5

GUDID 07290110722180

DENTAL IMPLANT

HI-TEC IMPLANTS LTD.

Transmandibular implant
Primary Device ID07290110722180
NIH Device Record Key89371545-cb5e-4841-8625-adc0fcbe8ac1
Commercial Distribution StatusIn Commercial Distribution
Brand NameTRI
Version Model NumberTRI-11.5mm
Catalog NumberTRI-11.5
Company DUNS600710917
Company NameHI-TEC IMPLANTS LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
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
GS107290110722180 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-05-22

On-Brand Devices [TRI]

07290110727482IMPLANT ANALOG
07290110726928NYLON COPING
07290110722210DENTAL IMPLANT
07290110722203DENTAL IMPLANT
07290110722197DENTAL IMPLANT
07290110722180DENTAL IMPLANT

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