LOSPA Knee System, EXULT Knee System

GUDID 08800017204871

Patella Peg Drill

Corentec Co., Ltd

Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable Fluted surgical drill bit, reusable
Primary Device ID08800017204871
NIH Device Record Key31cde672-de91-4815-a4a8-9864e2cdafdf
Commercial Distribution StatusIn Commercial Distribution
Brand NameLOSPA Knee System, EXULT Knee System
Version Model NumberKZ.020.0007
Company DUNS688739895
Company NameCorentec Co., Ltd
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
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+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com
Phone+820269374902
Emailra@corentec.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108800017204871 [Primary]

FDA Product Code

KIJInstrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


[08800017204871]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-01-23
Device Publish Date2024-01-15

On-Brand Devices [LOSPA Knee System, EXULT Knee System]

08800068981486Patella Clamp Stylus
08800017205267Patella Clamp Resection Guide Head 2
08800017205250Patella Clamp Resection Guide Head 1
08800017204871Patella Peg Drill

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