7 results
·
26ms
·
Sources: EU EUDAMED, US FDA
MODIFIED ANATOMIC POROUS REPLACEMENT APR ACETABULA
FDA 510(k)
FDA Class 3
·Orthopedic
LANDLEX MODEL S400X
FDA 510(k)
FDA Class 2
·Physical Medicine
RhythmStar System (SL)
FDA 510(k)
FDA Class 2
·Cardiovascular
ENDOSCOPE, UTEROSCOPE, VIPER
FDA Adverse Event
Malfunction
·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code FDC·March 21, 2014
UNKNOWN
FDA Adverse Event
Injury
·WRIGHT MEDICAL·Product code HTW·November 15, 2012
RESERVOIR 1.8ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 17, 2015
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021