64 results
·
31ms
·
Sources: EU EUDAMED, US FDA
MEDI-SIS SYRINGE INFUSION SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
Smith & Nephew, Inc.·00885556008201·BONE CURETTE STRAIGHT 228.6MM X
...
HUMMER IV MICRODEBRIDER SYSTEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
HORIZONTAL-VERTICAL LUMBAR VALVE AND SPETZLER LUMBAR PERITONEAL SHUNT SYSTEMS
FDA 510(k)
FDA Class 2
·Neurology
UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022
GYNECARE MORCELLEX* TISSUE MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code HET·May 14, 2013
INTERSTIM II
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·September 23, 2014
PINN MAR +4 10D 32IDX48OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·May 13, 2011
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code HWC·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 40
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 45
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 45
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 40
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
FINAL SCREWDRIVER SHAFT - II
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·February 15, 2016