Straight Abutment

GUDID 07290112280275

Straight Abutment

DENTACK IMPLANTS LTD

Screw endosteal dental implant, two-piece
Primary Device ID07290112280275
NIH Device Record Keydc513625-5d28-4913-a7d6-bb89dce19ea9
Commercial Distribution StatusIn Commercial Distribution
Brand NameStraight Abutment
Version Model NumberSA-300
Company DUNS514897185
Company NameDENTACK 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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+97297660379
Emailinfo@pyramidion-is.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107290112280275 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07290112280275]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2018-02-23

On-Brand Devices [Straight Abutment]

07290112280299Straight Abutment
07290112280275Straight Abutment
07290112280251Straight Abutment
07290112280237Straight Abutment

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