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Kensington Medical Holdings, LLC

FDA UDI
KENSINGTON MEDICAL HOLDINGS LLC·00860005968657·Stainless Steel Insert Basket for Flash-Guard 20"

Kensington Medical Holdings, LLC

FDA UDI
KENSINGTON MEDICAL HOLDINGS LLC·00860005968640·Stainless Steel Insert Basket for Flash-Guard 14"

Kensington Medical Holdings, LLC

FDA UDI
KENSINGTON MEDICAL HOLDINGS LLC·00860005968633·Stainless Steel Insert Basket for Flash-Guard 12"

Kensington Medical Holdings, LLC

FDA UDI
KENSINGTON MEDICAL HOLDINGS LLC·00860005968664·Stainless Steel Insert Basket for Flash-Guard 23"

COAPTITE INJECTABLE IMPLANT

FDA Adverse Event
Other ·MERZ NORTH AMERICA. INC.·Product code LNM·October 29, 2014

LEKSELL GAMMA KNIFE PERFEXION

FDA Adverse Event
Death ·ELEKTA INSTRUMENT AB·Product code IWB·October 12, 2016

GAMMABEAM 100

FDA Adverse Event
Malfunction ·BEST THERATRONICS LTD.·Product code IWB·July 21, 2015

LEKSELL GAMMA KNIFE

FDA Adverse Event
Injury ·ELEKTA INSTRUMENT AB·Product code IWB·February 19, 2009

THERATRON

FDA Adverse Event
Malfunction ·BEST THERATRONICS LTD.·Product code IWB·May 13, 2014

ELEKTA GAMMAKNIFE, AB

FDA Adverse Event
Malfunction ·ELEKTA, AB·Product code IWB·January 26, 2010

LEKSELL GAMMA KNIFE

FDA Adverse Event
Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·March 1, 2010

LEKSELL GAMMA KNIFE PERFEXION

FDA Adverse Event
Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·June 2, 2014

LEKSELL GAMMA KNIFE

FDA Adverse Event
Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·June 15, 2010

ALCYON I

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS EUROPE·Product code IWB·September 30, 1996

LEKSELL GAMMAPLAN, KULA

FDA Adverse Event
Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·July 1, 1996

LEKSELL GAMMA KNIFE PERFEXION

FDA Adverse Event
Malfunction ·ELEKTA INSTRUMENT AB·Product code IWB·May 16, 2014

THERATRON

FDA Adverse Event
Malfunction ·BEST THERATRONICS LTD·Product code IWB·December 24, 2012

LEKSELL GAMMA KNIFE

FDA Adverse Event
Other ·ELEKTA INSTRUMENT, AB.·Product code IWB·April 26, 2012

LEKSELL GAMMA KNIFE

FDA Adverse Event
Other ·ELEKTA INSTRUMENT AB·Product code IWB·May 30, 2012

THERATRON

FDA Adverse Event
Other ·MDS NORDION·Product code IWB·January 28, 2002