8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
OES THORACOSCOPE SYSTEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
TELESCOPE, 10 MM, 0°, QUICK LOCK, AUTOCLAVABLE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·October 31, 2023
TELESCOPE, 10 MM, 30°, HD, QUICK LOCK, AUTOCLAVABLE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code EWY·June 5, 2023
C100 WRINKLE REDUCTION DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MODIFICATION TO VASCULAR CLOSURE DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ALCON
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HQL·May 29, 2014
SOLITAIRE REVASCULARIZATION DEVICE
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code NRY·July 14, 2015
PK DISSECTING FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·January 11, 2013