24 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Nanovis Intervertebral Body Fusion System and FortiCore®
FDA 510(k)
FDA Class 2
·Orthopedic
LIPOSONIX SYSTEM, MODEL 1 P00XXXX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEPUY GLOBAL AP SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
INFINION 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 24, 2020
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·October 10, 2014
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Malfunction
·WAVELIGHT GMBH·Product code LZS·June 16, 2011
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·April 18, 2019
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·March 2, 2020
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·March 18, 2021
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·April 21, 2021
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·June 21, 2019
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·January 25, 2024
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·January 29, 2019
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·March 12, 2020
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·March 12, 2020
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·December 8, 2022
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·March 31, 2022
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·October 10, 2019
Artis zeego, Material no. 10280959 , for angiography and whole body radiographic/fluoroscopic procedures.
FDA Enforcement
Class II
·Terminated·Siemens Medical Solutions USA, Inc·July 4, 2018