10,000 results
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103ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Caliber Intramedullary Fixation System
FDA UDI
NVISION BIOMEDICAL TECHNOLOGIES, INC.·00810135963107·Caliber Kwire Guide
The Caliber Intramedullary ...
IJS
FDA UDI
SKELETAL DYNAMICS L.L.C.·00841506105154·IJS-E K-Wire Guide, 1.5mm
UNSPECIFIED OZARK SCREW
FDA Adverse Event
Malfunction
·K2M, INC.·Product code KWG·June 9, 2022
UNSPECIFIED OZARK SCREW
FDA Adverse Event
Malfunction
·K2M, INC.·Product code KWG·June 9, 2022
LEFT THUMB CONDYLAR IMPLANT
FDA Adverse Event
Malfunction
·UNKNOWN·Product code KWG·April 22, 1996
CMC, TRAPEZIUM SIZE 20
FDA Adverse Event
Injury
·STRYKER GMBH·Product code KWG·November 17, 2017
TSRH 3D 6.5 X 50 MM SCREW, TI
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEKMANUFACTURING·Product code KWG·August 19, 2004
UNSPECIFIED OZARK SCREW
FDA Adverse Event
Malfunction
·K2M, INC.·Product code KWG·June 9, 2022
UNKNOWN ARPE CUP
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWG·April 1, 2019
UNKNOWN ARPE STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWG·April 1, 2019
UNKNOWN ARPE NECK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWG·April 1, 2019
AE-QAS-SP42
FDA Adverse Event
Injury
·AESCULAP AG·Product code KWG·March 4, 2024
AE-QAS-SP42
FDA Adverse Event
Injury
·AESCULAP AG·Product code KWG·March 4, 2024
AE-QAS-SP42
FDA Adverse Event
Injury
·AESCULAP AG·Product code KWG·March 4, 2024
AE-QAS-SP42
FDA Adverse Event
Injury
·AESCULAP AG·Product code KWG·March 4, 2024
AE-QAS-SP42
FDA Adverse Event
Injury
·AESCULAP AG·Product code KWG·March 4, 2024
AE-QAS-SP42
FDA Adverse Event
Injury
·AESCULAP AG·Product code KWG·March 4, 2024
ARPE HEAD CURVE LONG +2
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code KWG·January 22, 2019
C8701, S ALEXIS LAP SYS W/KII FIOS 5/BX
FDA Adverse Event
Malfunction
·APPLIED MEDICAL RESOURCES·Product code KWG·August 30, 2019
C8402, M ALEXIS O WND PROT/RET 5/BX
FDA Adverse Event
Malfunction
·APPLIED MEDICAL RESOURCES·Product code KWG·December 13, 2019