10,000 results · 33ms · Sources: EU EUDAMED, 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