8 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Luvis Chair (LC700C)
FDA 510(k)
FDA Class 1
·Dental
PRECEPTIS TYMPANOSTOMY TUBE INSERTER
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
AMMONIA-L3K ASSAY, CATALOGUE NUMBER 233-10
FDA 510(k)
FDA Class 1
·Clinical Chemistry
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 22, 2025
BD¿ NESTABLE NON-VENT SHARPS COLLECTOR
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·June 21, 2023
PUNCH THRU TIBIAL BASE PLATE
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·November 14, 2008
ASR ACETABULAR IMPLANT 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·September 6, 2011
DUROM HIP
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·July 16, 2013