13 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STERIMATIC(TM) SAFETY NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
DGH A-SAN PROBE HOLDER
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 13, 2013
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·January 8, 2014
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·May 12, 2015
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·September 6, 2012
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 24, 2013
BIA400 IMPLANT 4MM W ABUTMENT 8MM
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·May 25, 2016
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·April 1, 2013
5 FR DL POWERPICC SOLO CATHETER, BASIC WITH
FDA Adverse Event
Malfunction
·C. R. BARD INC. (BASD)·Product code LJS·January 3, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·November 15, 2010
IROX
FDA Adverse Event
Injury
·GUIDANT ANGLETON/ST. PAUL·Product code DTB·July 1, 2014