1,049 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
K-WIRE / DZK
FDA Adverse Event
Injury
·BROOKS MANUFACTURING SITE·Product code DZK·May 11, 2009
HA COATED HALF PINS
FDA Adverse Event
Injury
·SMITH & NEPHEW·Product code DZK·May 5, 2014
UNKNOWN TOGGLELOC
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code DZK·October 11, 2021
PINS/WIRES
FDA Adverse Event
Injury
·SYNTHES USA·Product code DZK·May 3, 2012
CABLE/WIRE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code DZK·May 10, 2012
PINS/WIRES
FDA Adverse Event
Injury
·Product code DZK·June 4, 2012
K-WIRE
FDA Adverse Event
Injury
·STRYKER INSTRUMENTS·Product code DZK·September 17, 2003
K-WIRES
FDA Adverse Event
Injury
·STRYKER INSTRUMENTS·Product code DZK·September 17, 2003
UNK
FDA Adverse Event
Other
·UNK·Product code DZK·August 25, 2003
TRUE/LOK EXTERNAL FIXATION SYSTEM WIRE
FDA Adverse Event
Malfunction
·ORTHOFIX INC.·Product code DZK·November 13, 2008
PINS/WIRES
FDA Adverse Event
Injury
·SYNTHES USA·Product code DZK·December 13, 2012
WIRE
FDA Adverse Event
Injury
·Product code DZK·October 5, 2012
WIRE/PIN
FDA Adverse Event
Injury
·SYNTHES USA·Product code DZK·November 9, 2012
K-WIRE 10/10 - LENGTH 70 MM
FDA Adverse Event
Malfunction
·INTEGRA, SAINT PRIEST·Product code DZK·April 8, 2011
2.8MM THREADED GUIDE WIRE 450MM/TROCAR POINT
FDA Adverse Event
Malfunction
·Product code DZK·February 27, 2013
WIRE, FIXATION, INTRAOSSEOUS
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code DZK·November 27, 2018
WIRE BAY PT CORTICAL 370MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code DZK·February 27, 2013
WIRE, FIXATION, INTRAOSSEOUS
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code DZK·March 7, 2014
CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZK·February 7, 2014
SMOOTH WIRES
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code DZK·June 27, 2013