15 results
·
33ms
·
Sources: EU EUDAMED, US FDA
UREA AGAR BASE
FDA 510(k)
FDA Class 1
·Microbiology
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756600668·Electrode, Lletz
VISTASEAL LAPAROSCOPIC DUAL APPLICATOR (45 CM FLEXIBLE)
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MZM·August 25, 2025
VISTASEAL LAPAROSCOPIC DUAL APPLICATOR (45 CM FLEXIBLE)
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MZM·September 10, 2025
GENESIS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Neurosign V4 Intraoperative Nerve Monitor
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
VISTASEAL LAPAROSCOPIC DUAL APPLICATOR (45 CM FLEXIBLE)
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MZM·September 23, 2025
VISTASEAL LAPAROSCOPIC DUAL APPLICATOR (45 CM FLEXIBLE)
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MZM·August 25, 2025
VISTASEAL LAPAROSCOPIC DUAL APPLICATOR (45 CM FLEXIBLE)
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MZM·September 23, 2025
VISTASEAL LAPAROSCOPIC DUAL APPLICATOR (45 CM FLEXIBLE)
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MZM·September 23, 2025
VISTASEAL LAPAROSCOPIC DUAL APPLICATOR (45 CM FLEXIBLE)
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MZM·September 23, 2025
ETHILON NYLON SUTURE
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAR·June 18, 2014
LIFEPAK 1000 DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·October 20, 2010
LENSX LASER SYSTEM
FDA Adverse Event
Injury
·ALCON - LENSX LASERS, INC.·Product code OOE·December 17, 2012
VISTASEAL LAPAROSCOPIC DUAL APPLICATOR (45 CM FLEXIBLE)
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code MZM·July 8, 2025