7,375 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COMPOLGLASS COMPOGLASS SCA
FDA 510(k)
FDA Class 2
·Dental
Tissue-Tek® SCA™
FDA UDI
SAKURA FINETEK U.S.A., INC.·00615233078896·Coverslipping Film Cutter Blades; 5/cs
SAKURA-MEDSCAND SCA-1800 AUTOMATIC COVERSLIPPER
FDA 510(k)
FDA Class 1
·Pathology
SELF THREAD/LOGIC PLUS/SPARK
FDA UDI
HI-TEC IMPLANTS LTD.·07290110724535·SCREW-IN ABUTMENT
Conical Abutment Screw NP
FDA UDI
QUICKDENT DEVICES PRIVATE LIMITED·D16900SCANP0·
Conical Abutment Screw RP
FDA UDI
QUICKDENT DEVICES PRIVATE LIMITED·D16900SCARP0·
Blossom
FDA UDI
INTRA-LOCK INTERNATIONAL, INC.·D742SCA0·Gs Plastic Castable Abutment, w/ Retaining Screw
NEUROMED MODEL OCA-30 OCTODE AND MODEL SCA-30
FDA 510(k)
FDA Class 2
·Neurology
SET ZZ BASE AG-AX-WSM SCA
FDA UDI
ZIRKONZAHN SRL·D800ZBCD8332·SET ZZ BASE AG-AX-WSM SCA (White Scanmarker and...
ZIPWIRE HYDROPHILIC GUIDE WIRE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·August 9, 2012
PULSERIDER T, 4MM, 8MM ARCH
FDA Adverse Event
Injury
·PULSAR VASCULAR·Product code NJE·October 10, 2018
PULSERIDER Y, 4MM, 8MM ARCH
FDA Adverse Event
Injury
·PULSAR VASCULAR·Product code NJE·October 10, 2018
ENDURANT II EXTENSION STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·March 3, 2017
TRX
FDA UDI
HI-TEC IMPLANTS LTD.·07290110724610·SCREW-IN ABUTMENT
Sinus Stopper
FDA UDI
WARANTEC.Co.,Ltd·08800026122180·
DIO BIOTITE-H IMPLANT SYSTEMS
FDA UDI
DIO Corporation·08806195925690·The DIO Biotite-H Implant System is comprised o...
Nellcor
FDA UDI
Covidien LP·20884522042458·Adult SpO2 Sensor Non-Adhesive
Sinus Stopper
FDA UDI
WARANTEC.Co.,Ltd·08800026122173·
Sinus Stopper
FDA UDI
WARANTEC.Co.,Ltd·08800026122210·
Sinus Stopper
FDA UDI
WARANTEC.Co.,Ltd·08800026122265·