INCLUSIVE DRILL EXTENDER 70-1071-SRG0014

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-17 for INCLUSIVE DRILL EXTENDER 70-1071-SRG0014 manufactured by Prismatik Dentalcraft, Inc..

MAUDE Entry Details

Report Number3011649314-2019-00331
MDR Report Key8798615
Date Received2019-07-17
Date of Report2019-07-17
Date of Event2019-06-21
Date Mfgr Received2019-06-21
Device Manufacturer Date2019-04-05
Date Added to Maude2019-07-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. HERBERT SCHOENHOEFER
Manufacturer Street2212 DUPONT DRIVE SUITE P
Manufacturer CityIRVINE CA 92612
Manufacturer CountryUS
Manufacturer Postal92612
Manufacturer Phone9494402632
Manufacturer G1PRISMATIK DENTALCRAFT, INC.
Manufacturer Street2212 DUPONT DR SUITE P
Manufacturer CityIRVINE CA 92612
Manufacturer CountryUS
Manufacturer Postal Code92612
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameINCLUSIVE DRILL EXTENDER
Generic NameINCLUSIVE DRILL EXTENDER
Product CodeDZA
Date Received2019-07-17
Model Number70-1071-SRG0014
Catalog Number70-1071-SRG0014
Lot Number6069352
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerPRISMATIK DENTALCRAFT, INC.
Manufacturer Address2212 DUPONT DRIVE SUITE P IRVINE CA 92612 US 92612


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-17

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