13 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RELIATACK ARTICULATING RELOADABLE FIXATION DEVICE WITH STANDARD PURCHASE ABSORBLE TACKS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ZAVATION F3D-Z CIF
FDA UDI
Zavation LLC·00197157020958·F3D-Z CIF 16mmx18mmx9mm - 6deg
INTREPED, Intraosseous Fusion Device
FDA UDI
Auxano Medical LLC·00850055649385·INTREPED 09 Tap (Beta)
Humelock II Cemented Reversible Shoulder
FDA UDI
FX SOLUTIONS·03701037302927·HUMERAL CUP 135/145° MOBILITY PE/TA6V Ø40 +9
Humelock II Cemented Reversible Shoulder
FDA UDI
FX SOLUTIONS·03701037308264·TRIAL HUMERAL CUP 135/145° MOBILITY Ø40 +9
NUCLEUS CI512 COCHLEAR IMPLANT WITH CONTOUR ADVANCE ELECTRODE
FDA Adverse Event
Malfunction
·COCHLEAR LTD·Product code MCM·April 28, 2019
EPIDUCER LEAD DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
RAPID PROGRAMMER
FDA 510(k)
FDA Class 2
·Neurology
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LGW·September 9, 2022
INFANT DUAL HEATED EVAQUA2 BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·October 21, 2014
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTP·May 31, 2013
MELODY TRANSCATHER PULMONARY
FDA Adverse Event
Malfunction
·MEDTRONIC HEART VALVES DIVISION·Product code NPV·October 3, 2014
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·June 16, 2011