Angled Abutment

GUDID 07290112280039

Angled Abutment for EX

DENTACK IMPLANTS LTD

Screw endosteal dental implant, two-piece
Primary Device ID07290112280039
NIH Device Record Key2c6b2c88-2c1a-4c4b-a49d-c054a38f5ad1
Commercial Distribution StatusIn Commercial Distribution
Brand NameAngled Abutment
Version Model NumberAA-150EX
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
GS107290112280039 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07290112280039]

Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-02-28
Device Publish Date2019-01-28

On-Brand Devices [Angled Abutment]

07290112280077Angled Abutment for EX
07290112280060Angled Abutment
07290112280053Angled Abutment for EX
07290112280046Angled Abutment
07290112280039Angled Abutment for EX
07290112280022Angled Abutment

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