10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
SYMBIOSIS BONE MARROW BIOPSY NEEDLE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
FYMCO FLYER
FDA 510(k)
FDA Class 2
·Physical Medicine
VESSEL DILATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
STYLE 68 SALINE FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FWM·July 12, 2022
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·September 22, 2012
ARTICULEZE M HEAD 36MM +12
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 22, 2012
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·June 18, 2014
LIGAMAX-5MM ENDO CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·December 14, 2010
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·January 22, 2013
MENTOR SMOOTH ROUND MODERATE PROFILE SALINE BREAST PROSTHESIS
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·March 5, 2026