TRX-TP TP-SCA

GUDID 07290110724627

SCREW-IN ABUTMENT

HI-TEC IMPLANTS LTD.

Dental implant suprastructure, permanent, preformed
Primary Device ID07290110724627
NIH Device Record Keya86ce3ec-8c80-4cb3-bde9-5c25696a85c7
Commercial Distribution StatusIn Commercial Distribution
Brand NameTRX-TP
Version Model NumberTP-SCA
Catalog NumberTP-SCA
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 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
GS107290110724627 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-08
Device Publish Date2017-06-08

On-Brand Devices [TRX-TP]

07290110726690BALL-ATTACHMENT ABUTMENT
07290110726683BALL-ATTACHMENT ABUTMENT
07290110726355FIXED DETACHABLE ABUTMENT
07290110724627SCREW-IN ABUTMENT
07290110722135DENTAL IMPLANT
07290110722128DENTAL IMPLANT
07290110722111DENTAL IMPLANT
07290110722104DENTAL IMPLANT
07290110722098DENTAL IMPLANT
07290110722081DENTAL IMPLANT
07290110722074DENTAL IMPLANT
07290110722067DENTAL IMPLANT

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.