8 results
·
24ms
·
Sources: EU EUDAMED, US FDA
TECA/MEDELEC 'CONCEPT' P420
FDA 510(k)
FDA Class 2
·Neurology
SUNTAN CONNECTIONS BAHAMA SUN-BOOTH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
INTRAOCULAR ELECTROMAGNET
FDA 510(k)
FDA Class 2
·Ophthalmic
M2A-MAGNUM PF CUP 58ODX52ID
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 19, 2014
DRIVER SPRINT RX CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MAF·October 15, 2010
STENOSCOP
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 3, 2012
MODULAR NECK G2 12/14 NECK TAPER USE WITH +0 HEADS ONLY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·January 10, 2020
FEMORAL HEAD STERILE PRODUCT 12/14 TAPER
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·January 10, 2020