GUDID 06009544021568

Titanium Abutment, Non-Engaging, for Ø4.0 Ex Hex, 1mm Cuff

SOUTHERN IMPLANTS (PTY) LTD

Dental implant suprastructure, permanent, preformed
Primary Device ID06009544021568
NIH Device Record Key813d1b81-8140-4d95-8317-8d445563593f
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberTCB1NH
Company DUNS636239584
Company NameSOUTHERN IMPLANTS (PTY) 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 Datefalse
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
GS106009544021568 [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 Number2
Public Version Date2019-11-08
Device Publish Date2019-01-21

Devices Manufactured by SOUTHERN IMPLANTS (PTY) LTD

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06009544027652 - N/A2025-04-10 Resorbable collagen membrane 30x40mm
06009544027669 - N/A2025-04-10 Bone matrix, porcine cancellous fine 0.5cc
06009544027676 - N/A2025-04-10 Bone matrix, porcine cancellous fine 1.0cc
06009544027683 - N/A2025-04-10 Bone matrix, porcine cancellous fine 2.0cc
06009544027690 - N/A2025-04-10 Bone matrix, porcine cancellous std 2.0cc
06009544027706 - N/A2025-04-10 Bone matrix, porcine cancellous std 1.0cc

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