7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
CLOTHINGUARD
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
UROL-QUAL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
CHURCHHILL LANCET
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OPTIFLUX F250NRE DIALYZER
FDA Adverse Event
Malfunction
·OGDEN MANUFACTURING·Product code KDI·May 19, 2014
3 MOTOR ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·November 5, 2010
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·December 20, 2012
BIOMET StageOne Knee Femoral Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 432170.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020