24 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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QUICKCLOT
FDA 510(k)
FDA Unclassified
·Unknown
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021565720·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021565737·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0133000·Assembly, Rod Reducer, Ratcheting
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021565751·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021565744·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021565713·
MAGNIVISION
FDA UDI
FGX INTERNATIONAL INC.·00024021565775·
BONUS-ORTHOPEDIC BONE SCREW FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS
FDA 510(k)
FDA Class 2
·Cardiovascular
UNK COMP LOCKING SCREW
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·March 10, 2014
XIA 3 TITANIUM TORQUE WRENCH
FDA Adverse Event
Malfunction
·STRYKER SPINE-FRANCE·Product code LXH·March 20, 2013
COBAS 6000 E601 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JHI·March 10, 2011
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 10, 2008
ACIST
FDA Adverse Event
Injury
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012
OPTILENE 6/0 (0,7) 75CM 2XDRC10 CV RCP
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAW·December 6, 2019
ACIST
FDA Adverse Event
Malfunction
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007
ACIST
FDA Adverse Event
Injury
·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012
OPTILENE 6/0 (0,7) 45CM DS16 (M) RCP
FDA Adverse Event
Malfunction
·B/ BRAUN SURGICAL SA·Product code GAW·July 22, 2019
OPTILENE 6/0 (0,7) 45CM DS16 (M) RCP
FDA Adverse Event
Malfunction
·B/ BRAUN SURGICAL SA·Product code GAW·July 22, 2019