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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