33 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·November 18, 2015
SYNTHES 2.4 MM/2.7 MM VARIABLE ANGLE LCP FOREFOOT/MIDFOOT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·August 3, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·August 4, 2015
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·October 8, 2015
VA LOCKSCR Ø2.4 SELF-TAP L24 TAN
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·December 9, 2013
VA LOCKSCR Ø2.4 SELF-TAP L24 TAN
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·December 9, 2013
2.4MM TI VA LOCKING SCREW STARDRIVE 22MM
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·December 9, 2013
2.7MM VA LCKNG SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 11MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HWC·December 22, 2014
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HRS·October 7, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·October 3, 2014
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 10, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·August 12, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·June 30, 2016
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·October 24, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·October 24, 2015
DEBAKEY SUBRAMANIAN AORTIC CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896091122·DEBAKEY SUBRAMANIAN AORTIC CLAMP ANGLED TIP
MICHEL WOUND CLIPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896090668·MICHEL WOUND CLIPS STAINLESS STEEL
DEBAKEY SUBRAMANIAN AORTIC CLAMP
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921007760·DEBAKEY SUBRAMANIAN AORTIC CLAMP ANGLED
Ear Tip PM107 Pack/100 pcs. (Grason)
FDA UDI
PATH medical GmbH·04260223142178·PATH MEDICAL is not manufacturer or Labeler of ...