10,000 results
·
72ms
·
Sources: EU EUDAMED, US FDA
Globus Medical, Inc.
Manufacturer
🇺🇸 United States·1 Importer
Globus Medical, Inc.
Device
EU MDD
·
Eu Md Class 2b
·Kirwan Surgical Products LLC·On the market·31 countries
Globus Medical, Inc
Device
EU MDD
·
Eu Md Class 2b
·Kirwan Surgical Products LLC·On the market·31 countries
GLOBUS MEDICAL, INC.
FDA registration
GLOBUS MEDICAL, INC.·77 products·🇺🇸 United States
GLOBUS MEDICAL, INC.
FDA registration
GLOBUS MEDICAL, INC.·86 products·🇺🇸 United States
GLOBUS MEDICAL, INC.
FDA registration
GLOBUS MEDICAL, INC.·6 products·🇺🇸 United States
GLOBUS MEDICAL, INC.
FDA Adverse Event
GLOBUS MEDICAL, INC.·Product code OVE·August 27, 2014
XPAND
FDA Adverse Event
Other
·GLOBUS MEDICAL, INC.·Product code MQP·October 7, 2006
4.0MM X 14MM RIGID SCREW, SELF-DRILLING
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code KWQ·May 21, 2009
4.0MM RIGID SCREW, SELF DRILLING, 16MM
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code KWQ·May 7, 2009
4.5MM X 16MM STANDARD SCREW, SELF-DRILLING
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code KWQ·May 22, 2009
5.5MM STRAIGHT ROD, 400MM
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code KWQ·May 4, 2009
4.0MM RIGID SCREW, SELF DRILLING, 16MM
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code KWQ·May 7, 2009
DEVICE TWO:5.5MM REVERE PEDICLE SCREW
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code MNH·June 18, 2009
XPAND CORPECTOMY SPACER MEDIUM 21X23 -3/3 DEGREES 3
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code MQP·June 18, 2009
GLOBUS MEDICAL INC. POSTERIOR SPINAL FUSION
FDA Adverse Event
Malfunction
·GLOBUS MEDICAL INC.·Product code NQP·October 4, 2021
XPAND SPACER LARGE 25X32 4/4 39-41MME
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code MQP·November 26, 2008
6.5MM REVERE PEDICLE SCREW 45MM
FDA Adverse Event
Other
·GLOBUS MEDICAL, INC.·Product code MCV·August 30, 2007
SIGNATURE TLIF SPACER, SMALL, 12MM
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code KWQ·May 29, 2009
INTERCONTINENTAL
FDA Adverse Event
Malfunction
·GLOBUS MEDICAL, INC.·Product code LXH·February 29, 2024