8 results
·
34ms
·
Sources: EU EUDAMED, US FDA
CENTRAL PEG TIBIAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
PROXIMAL HUMERUS SCAFFOLD FIXATION SYSTEM (PHSFS)
FDA 510(k)
FDA Class 2
·Orthopedic
Disposable Standard Clamp
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PINNACLE MTL INS NEUT36IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·April 30, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 12, 2007
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 10, 2012
TITAN TOUCH
FDA Adverse Event
Injury
·COLOPLAST A/S·Product code FHW·March 1, 2022
PROPONENT DR SL (Model L201)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025