27 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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COOL LINE CATHETER, MODEL CL-2295A, ICY CATHETER, MODEL IC-3893A AND QUATTRO CATHETER, MODEL IC-4593
FDA 510(k)
FDA Class 2
·Cardiovascular
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964072864·The ENDO CARRY-ON Procedure Kit contains all of...
EXPLORER GRADIENT
FDA 510(k)
FDA Class 2
·Radiology
MODIFIED M-IV MAMMOGRAPHY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
IMP,TSV,4.7,10,MTX,MG
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·May 22, 2026
IMP,TSV,4.7,11.5,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·June 12, 2024
IMP,TSV,4.7,10,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·October 28, 2024
SEALING UNIT FROM 5MM TROCARS
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GCJ·June 17, 2015
REDUCING CONVERTER 10/12MM TO 5MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GCJ·June 17, 2015
IMP,TSV,4.7,8,MTX,MG
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·April 22, 2026
IMP,TSV,6.0,11.5,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·May 15, 2025
IMP,TSV,3.7,8,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·July 12, 2024
IMP,TSV,4.7,10,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·June 10, 2024
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 3, 2013
ALARIS PCA MODULE
FDA Adverse Event
Malfunction
·CAREFUSION CORP·Product code MEA·May 19, 2011
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·August 6, 2008
IMP,TSV,4.7,11.5,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·November 6, 2024
IMP,TSV,4.7,8,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·November 8, 2024
IMPL TAPERED SCR-V SBM 3. 7MM 3.5MM 8MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·October 4, 2023
IMP,TSV,4.7,8,MTX,MG
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·March 17, 2026