10,000 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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U.S. IOL, Inc.
FDA UDI
U.S. IOL, INC.·00814106015949·6/0 Micro Spatula, Double-Armed Nylon Suture
U.S. IOL, Inc.
FDA UDI
U.S. IOL, INC.·00814106015987·8/0 Micro Spatula, Double-Armed Nylon Suture
U.S. IOL, Inc.
FDA UDI
U.S. IOL, INC.·00814106015963·7/0 Taper Point, Double-Armed Nylon Suture
U.S. IOL, Inc.
FDA UDI
U.S. IOL, INC.·00814106016007·9/0 Micro Spatula, Double-Armed Nylon Suture
RV. UNIVERSAL CEMENT RESTRICTOR
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS·Product code LZN·February 5, 2010
NONE
FDA Adverse Event
Injury
·ISOTIS ORTHOBIOLOGICS, INC·Product code LZN·July 13, 2015
SYNPLUG -UNKNOWN SIZE
FDA Adverse Event
Injury
·ISOTIS ORTHOBIOLOGICS, INC·Product code LZN·July 14, 2015
MEDULLARY PLUG WITH DRAIN 3.5
FDA Adverse Event
Death
·ZIMMER GMBH·Product code LZN·July 2, 2015
SYNPLUG -UNKNOWN SIZE
FDA Adverse Event
Injury
·ISOTIS ORTHOBIOLOGICS, INC·Product code LZN·July 14, 2015
MED HOWMEDICA BONE PLUG 1PK
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS CORK·Product code LZN·January 10, 2012
12X100MM KII Z-THREAD ACC SYS W/SHLD BLD OBTURATOR
FDA Adverse Event
APPLIED MEDICAL·Product code LZN·January 4, 2012
12X100MM KII Z-THREAD ACC SYS W/SHLD BLD OBTURATOR
FDA Adverse Event
APPLIED MEDICAL·Product code LZN·March 14, 2012
12X100MM KII Z-THREAD ACC SYS W/SHLD BLD OBTURATOR
FDA Adverse Event
Other
·APPLIED MEDICAL·Product code LZN·February 15, 2012
OSTEONIC UNIV. DISTAL SPACER
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS MAHWAH·Product code LZN·March 30, 2010
SYNPLUG SIZE 16
FDA Adverse Event
Injury
·ISOTIS ORTHOBIOLOGICS, INC·Product code LZN·April 9, 2014
EXETER 2.5 I M PLUG 14MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS LIMERICK·Product code LZN·June 1, 2010
EXETER 2.5 I M PLUG 16MM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS LIMERICK·Product code LZN·May 26, 2010
SYNPLUG - UNKNOWN SIZE
FDA Adverse Event
Injury
·ISOTIS ORTHOBIOLOGICS, INC·Product code LZN·September 16, 2015
SYNPLUG - UNKNOWN SIZE
FDA Adverse Event
Injury
·ISOTIS ORTHOBIOLOGICS, INC·Product code LZN·August 13, 2015
NONE
FDA Adverse Event
Injury
·ISOTIS ORTHOBIOLOGICS, INC·Product code LZN·July 13, 2015