10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
OUCHLESS MODEL PN10114
FDA 510(k)
FDA Unclassified
·Unknown
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450658109·
PECTOFIX STERNAL REPAIR WIRE
FDA 510(k)
FDA Class 2
·Orthopedic
SANDHILL SCIENTIFIC PEDIATEC PH PROBE
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·February 18, 2026
GRANUFLO
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 1, 2013
EXTRACTION SCREWDRIVER
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·September 16, 2014
LIGHTSPEED VCT
FDA Adverse Event
Other
·GE MEDICAL SYSTEMS, LLC·Product code JAK·April 22, 2011
ARCHITECT HE4 REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code OIU·February 6, 2026
M2A MAGNUM TAPER ADAPTER 52-60MM MINUS 3MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·October 8, 2018