8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VESITEC SUTURE PASSER
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
EXTERNAL FIXATION SYSTEMS
FDA 510(k)
FDA Class 2
·Orthopedic
OMEGA LABORATORIES HAIR DRUG SCREENING ASSAY PHENCYCLIDINE
FDA 510(k)
FDA Unclassified
·Unknown
E1 RINGLOC BIPOLAR 28X51MM
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LZO·June 17, 2019
BIOMEX SHELL PC DIA48MM LN 22
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·December 2, 2015
COMBISET WITH BVM
FDA Adverse Event
Malfunction
·REYNOSA MANUFACTURING·Product code FJK·November 16, 2010
REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 10
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 28, 2013
BLAZER® II
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - COSTA RICA (HEREDIA)·Product code LPB·July 14, 2014