8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
FLUTED SUCTION MENISCAL CUTTER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
FORMAGRAFT COLLAGEN BONE GRAFT MATRIX
FDA 510(k)
FDA Class 2
·Orthopedic
SPINAUT-E, SPINAUT-I
FDA 510(k)
FDA Class 2
·Anesthesiology
VACCESS PTA BALLOON DILATION CATHETER
FDA Adverse Event
Injury
·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·March 20, 2014
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - GUANGZHOU·Product code KDI·November 29, 2012
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 17, 2015
DEEP BRAIN STIMULATION LEAD
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·January 29, 2008
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021