10 results
·
28ms
·
Sources: EU EUDAMED, US FDA
PORTABLE LIFT SEAT
FDA 510(k)
FDA Class 2
·Physical Medicine
INSTAFLO BOWEL CATHETER SYSTEM KIT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MOSS MIAMI SPINAL SYSTEM PIN NUT
FDA 510(k)
FDA Class 2
·Orthopedic
LATERAL STRAIGHT STEM 15.0 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWB·March 28, 2012
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·January 22, 2013
CLEARLINK SYSTEM EXTENSION SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code FPA·December 14, 2010
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD .·Product code MCM·July 9, 2014
SULOX-HD 32 M 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·April 23, 2019
SULOX, HEAD, M¸ 32/0, TAPER 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWB·August 3, 2018
SULOX-HEAD 28 M 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LPH·April 4, 2019