10 results
·
27ms
·
Sources: EU EUDAMED, US FDA
EIA SMDP IMMUNOASSAY
FDA 510(k)
FDA Class 2
·Immunology
KD-931D FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
INNERBLOC LR SURGICAL GOWNS BASED ON GORE LR FABRIC (REUSABLE 100X)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MAYFIELD RADIOLUCENT BASE UNIT W/ADAPTORS
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·April 8, 2015
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FPO·May 1, 2013
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·June 17, 2011
BIOCOR STENTED PORCINE HEART VALVE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL BRASIL LTDA.·Product code LWR·August 22, 2008
THERMAGE CPT SYSTEM
FDA Adverse Event
Injury
·SOLTA MEDICAL, INC·Product code GEI·November 12, 2020
THERMAGE CPT SYSTEM TIP
FDA Adverse Event
Injury
·SOLTA MEDICAL INC·Product code GEI·November 30, 2022
Achieva 1.5T
FDA Enforcement
Class II
·Ongoing·Philips North America Llc·November 29, 2023