67 results
·
26ms
·
Sources: EU EUDAMED, US FDA
QLASER SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994877963·DRILL BIT 7080513 STERILE 13MM
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526827851·***DISC*LEVAMED ANKLE SUPPORT BLACK III
n/a
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000663865·DRILL BIT 7080513 STERILE 13MM
iTotal® Patella Trial
FDA UDI
Conformis, Inc.·00850268007125·iTotal® 41mm Patella Trial Reusable Instrument
Clamp, Hysterectomy, model Z 24cm angled
FDA UDI
Geister Medizintechnik GmbH·04057034373149·Clamp, Hysterectomy, model Z
24cm a...
CARDIAC VIEW, MODEL 2001
FDA 510(k)
FDA Class 2
·Radiology
MODIFICATION TO EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ARTICULEZE M HEAD 36MM +5 K980513
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 14, 2016
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 7, 2025
FREESTYLE LITE
FDA Adverse Event
Malfunction
·Product code NBW·April 26, 2013
HARMONIC ACE 36 CM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC·Product code LFL·July 24, 2008
LIGHTSPEED VCT
FDA Adverse Event
Injury
·GE MEDICAL SYSTEMS, LLC·Product code JAK·April 22, 2011
OT VITA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 20, 2010
OT VITA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 24, 2011
OT VITA ENHANCED METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·January 12, 2012
OT VITA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 21, 2011
OT VITA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 15, 2011
OT VITA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 14, 2010
OT VITA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·November 30, 2010