11 results
·
18ms
·
Sources: EU EUDAMED, US FDA
OPERAID SURGICAL DRAIN W/ CORNEAL SHIELDS
FDA 510(k)
FDA Class 2
·Ophthalmic
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756372862·NEURO PACK
ZAVATION
FDA UDI
Zavation LLC·00842166151819·WHITNEY 13mmx15mm , 7deg , 07mm
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668112328·SURG-I-BAND GREEN
ATLANTIS SR PLUS CORONARY IMAGING CATHETER, MODEL 35975
FDA 510(k)
FDA Class 2
·Cardiovascular
CARE BACK PAIN RELIEF STIMULATOR; CARE BACK PAIN RELIEF STIMULATOR
FDA 510(k)
FDA Class 2
·Neurology
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/12 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·December 18, 2020
EDWARDS SAPIEN XT TRANSCATHETER HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·June 6, 2017
CONTAK RENEWAL
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·January 11, 2013
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTR·November 22, 2010
SEVEN PLUS CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Injury
·DEXCOM, INC.·Product code MDS·July 2, 2014