8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-6000
FDA 510(k)
FDA Class 2
·Hematology
artegral life
FDA UDI
Merz Dental GmbH·D7091993174·anteriors; shade B1; mould BOS
SPIROPALM
FDA 510(k)
FDA Class 2
·Anesthesiology
Keos Lumbar IBFD
FDA 510(k)
FDA Class 2
·Orthopedic
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·March 18, 2025
MEDTRONIC INFUSE BONE GRAFT OR RHBMP2
FDA Adverse Event
MEDTRONIC, INC.·Product code NEK·February 27, 2013
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 7, 2011
CAPSURE SP NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·August 8, 2014