67 results · 26ms · Sources: EU EUDAMED, US FDA

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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