12 results
·
21ms
·
Sources: EU EUDAMED, US FDA
ESSAR TOURNIQUET FOR VENIPUNCTURE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
n.a.
FDA UDI
Karl Storz GmbH & Co. KG·04048551199831·Scissors, straight, 14.5 cm
Coblation
FDA UDI
Smith & Nephew, Inc.·00817470001419·PERC DC (OLD)
TIGRT MLC, TIGRT DMLC
FDA 510(k)
FDA Class 2
·Radiology
Envision ultrasound pad and cover
FDA 510(k)
FDA Class 2
·Radiology
SELF-RETAINING SCREWDRIVER FOR QUICK LOCK SCREWS 275MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·December 4, 2014
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·May 5, 2014
EXTERNAL PULSE GENERATOR
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012
EON IMPLANTABLE PULSE GENERATOR
FDA Adverse Event
Malfunction
·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·August 6, 2010
SELF-RETAINING SCREWDRIVER FORQUICK LOCK SCREWS 275MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·March 9, 2016
SURGICEL ABSORBABLE HEMOSTAT UNKNOWN
FDA Adverse Event
Death
·ETHICON INC.·Product code LMG·April 7, 2025
Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487, 100047194; CD3211-36Q/100004091, 100004093,100019784, 100035620, 100042486, 100047054; CD3215-36/100006995, 100010246, 100010247, 100010249, 100010250, 100012569, 100012570, 100034981, 100046577, 100046802, 60019065; CD3215-36Q/100004059, 100004060, 100004061, 100023304, 100030590, 100033678, 100042492, 100046803, 100046906
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018