42 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STINGRAY GUIDEWIRES
FDA 510(k)
FDA Class 2
·Cardiovascular
ArgenZ HT+ 95x25 B1
FDA UDI
ARGEN CORPORATION, THE·D818122795·Dental porcelain/ceramic restoration kit
MODIFICATION TO THE MAESTRO SYSTEM
FDA 510(k)
FDA Class 2
·Dental
SIGNATURE PLANNER; SIGNATURE GUIDES
FDA 510(k)
FDA Class 2
·Orthopedic
PROFEMUR(R) Z STEM
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·May 21, 2013
UNKNOWN DEPUY HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 3, 2011
FREESTYLE FREEDOM
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 13, 2008
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·May 12, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 25, 2017
AGC DA2000 KN TIB BRG 71/75X8
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·April 9, 2026
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 8, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·March 7, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·August 27, 2020
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·April 24, 2019
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·April 18, 2019
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·July 25, 2018
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·April 12, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·January 15, 2020
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·February 17, 2020
VANGUARD ROCC POR FEM S55 R
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code MBH·January 22, 2026