23 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Stay Fresh Hydrocolloid dressing
FDA 510(k)
FDA Unclassified
·Unknown
HHM
FDA UDI
Oticon A/S·05707131280107·H110, DESIGNRITE 10 WL MOP HHM
3.5MM CORTEX SCREW SELF-TAPPING 55MM
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code HWC·January 26, 2017
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·July 25, 2018
MICROPULSE PHACOEMULSIFICATION SYSTEM
FDA 510(k)
FDA Class 2
·Ophthalmic
AFFINITY VARD SUB-ASSEMBLY FOR CPS (CARMEDA COATED), PURGELINE (UNCOATED), HOLDING BAG
FDA 510(k)
FDA Class 2
·Cardiovascular
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·November 18, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 7, 2018
3.5MM CORTEX SCREW SELF-TAPPING 16MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 6, 2016
3.5MM CORTEX SCREW SELF-TAPPING 14MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 6, 2016
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013
S-ROM HEAD FEMORAL COCR 32+3
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code JDG·June 30, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 9, 2008
CORTSCR 3.5 SELF-TAP L65 TI
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code HWC·April 29, 2013
3.5MM CORTEX SCREW SELF-TAPPING 22MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·December 21, 2015
SUBDURAL ELECTRODE
FDA Adverse Event
Malfunction
·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GYC·August 18, 2025
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·January 4, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·July 14, 2016
3.5MM TI CORTEX SCREW 36MM
FDA Adverse Event
Malfunction
·SYNTHES TRAUMA : OBERDORF : SYNTHES PRODUKTIONS GM·Product code HWC·February 9, 2018
C-QUR MOSAIC
FDA Adverse Event
Injury
·ATRIUM MEDICAL CORPORATION·Product code FTL·October 9, 2015