415 results · 27ms · Sources: EU EUDAMED, US FDA

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MEDTRONIC NAVIGATION

FDA Adverse Event
Injury ·MEDTRONIC NAVIGATION, INC (LITTLETON)·Product code OXO·October 28, 2020

CORE INTRA-ORAL BLADE

FDA Adverse Event
Malfunction ·STRYKER·Product code DZH·March 14, 2009

CORE INTRA-ORAL BLADE

FDA Adverse Event
Malfunction ·STRYKER IRELAND LTD.·Product code DZH·June 17, 2010

TPS OSC SAW

FDA Adverse Event
Injury ·STRYKER INSTRUMENTS·Product code DZH·March 9, 2004

TPS OSCILLATING SAW

FDA Adverse Event
Injury ·STRYKER INSTRUMENTS·Product code DZH·September 16, 2003

MICROCHOICE INTRA ORAL BLADE 11.5X7 X 4MM

FDA Adverse Event
Malfunction ·CONMED LINVATEC·Product code DZH·June 7, 2007

MICROCHOICE INTRA ORAL BLADE 11.5X7 X 4MM

FDA Adverse Event
Malfunction ·CONMED LINVATEC·Product code DZH·June 5, 2007

MICRO OSCILLATING SAW

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZH·December 16, 2010

HALL LARGE BONE OSCILLATING BLADE

FDA Adverse Event
Malfunction ·CONMED LINVATEC·Product code DZH·November 30, 2007

HALL LARGE BONE OSCILLATING BLADE

FDA Adverse Event
Malfunction ·CONMED LINVATEC·Product code DZH·November 30, 2007

CORE INTRA-ORAL BLADE

FDA Adverse Event
Malfunction ·STRYKER IRELAND LTD.·Product code DZH·December 8, 2010

CORE INTRA-ORAL BLADE

FDA Adverse Event
Malfunction ·STRYKER IRELAND LTD·Product code DZH·April 3, 2009

SAW

FDA Adverse Event
Malfunction ·STRYKER·Product code DZH·October 10, 2000

SAWBLADE NEW Z STYLE 25WX050

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS·Product code DZH·September 1, 2004

OSTEOMED

FDA Adverse Event
Malfunction ·OSTEOMED CORP.·Product code DZH·May 27, 1997

TPS OSCILLATING SAW

FDA Adverse Event
Injury ·STRYKER INSTRUMENTS·Product code DZH·July 24, 2002

REPROCESSED STRYKER STERNUM SAW BLADE

FDA Adverse Event
Malfunction ·STERILMED, INC.·Product code DZH·December 11, 2007

REPAIR TPS OSC SAW

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZH·September 22, 2009

CORE INTRA-ORAL BLADE;OSCILLATING 7MM SAW BLADE

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS·Product code DZH·July 11, 2009

OSCILLATING SAW RETROFIT

FDA Adverse Event
Injury ·STRYKER INSTRUMENTS·Product code DZH·February 26, 1997