191 results · 32ms · Sources: EU EUDAMED, US FDA

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CONCENTRIC BALLOON GUIDE CATHETER, MODEL 90072

FDA 510(k)
FDA Class 2 ·Cardiovascular

LANTOR (UK), LTD.

FDA registration
LANTOR (UK), LTD.·3 products·🇬🇧 United Kingdom

IMPROVED TRY-IN GEL

FDA 510(k)
FDA Class 2 ·Dental

PF 5050 PRESSURE UNIT, MODEL PF 5050

FDA 510(k)
FDA Class 2 ·Cardiovascular

PARAPAC 'MEDIC' (K020899)

FDA Adverse Event
Death ·SMITHS MEDICAL INTERNATIONAL·Product code BTL·August 6, 2004

SEE H10

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KXA·November 1, 2011

SPECTRA WAVEWRITER?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 3, 2025

DEXTRUS 4135

FDA Adverse Event
Injury ·BIOTRONIK SE & CO. KG·Product code NVN·March 26, 2013

UNO

FDA Adverse Event
Malfunction ·LIKO AB·Product code FSA·March 11, 2011

8.0MM TI PANGEA POLYAXIAL

FDA Adverse Event
Malfunction ·SYNTHES BRANDYWINE·Product code KWP·March 28, 2008

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 16, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·November 11, 2010

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 23, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·May 9, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 18, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 16, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 2, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·October 5, 2010

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 10, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 17, 2011