188 results · 24ms · Sources: EU EUDAMED, US FDA

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AARON A950 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A950 ELECTROSURGICAL GENERATOR, 240V

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DUCKWORTH & KENT, LTD.

FDA registration
DUCKWORTH & KENT, LTD.·20 products·🇬🇧 United Kingdom

HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED

FDA 510(k)
FDA Class 2 ·Orthopedic

BRIDGE FX

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

SETROX S 60

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

STENOSCOP

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD.·Product code JAA·February 25, 2011

FORTIFY DR, DF-4 CONNECTOR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·August 19, 2014

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

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 2, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 14, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·June 6, 2011