195 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Stimulator, Hypoglossal Nerve, Implanted, Apnea
FDA Pre-Market Approval
FDA Class 3
·Genio® System 2.1
Stimulator, Hypoglossal Nerve, Implanted, Apnea
FDA Pre-Market Approval
FDA Class 3
·Genio® System 2.1
Stimulator, Hypoglossal Nerve, Implanted, Apnea
FDA Pre-Market Approval
FDA Class 3
·Genio® System 2.1
Stimulator, Hypoglossal Nerve, Implanted, Apnea
FDA Pre-Market Approval
FDA Class 3
·Genio® System 2.1
SpheRx
FDA UDI
Nuvasive, Inc.·00887517440242·SpheRx II Counter Torque
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·00636257009727·30-40 DUAL LAYER CALF SINGLE BEIGE L
3.2 / 6.0mm DOUBLE DRILL GUIDE
FDA UDI
Osteocentric Technologies, Inc.·00810189110533·3.2 / 6.0mm DOUBLE DRILL GUIDE
Amplatz
FDA UDI
COOK INCORPORATED·00827002180086·Amplatz Renal Introducer
PORTEX CO2 CLIP
FDA Adverse Event
Death
·SMITHS MEDICAL ASD, INC.·Product code CCK·November 9, 2005
AMS 800 URINARY CONTROL SYSTEM WITH INHIBIZONE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code EZY·November 13, 2018
130 DEG AIMING ARM F/TROCHANTERIC FIXATION NAILS
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code FZX·April 15, 2013
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·April 13, 2012
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·May 16, 2008
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·March 29, 2007
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·April 14, 2011
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LMH·November 26, 2008
RESTYLANE INJECTABLE GEL
FDA Adverse Event
Other
·Q-MED AB·Product code LNM·March 29, 2007
UNICEL® DXC 800 SYNCHRON® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·September 8, 2011
PASS LP
FDA Adverse Event
Injury
·MEDICREA INTERNATIONAL·Product code MNI·November 10, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·July 22, 2013