32 results · 25ms · Sources: EU EUDAMED, US FDA

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SYNTHES (USA) 3.5MM LCP HOOK PLATE

FDA 510(k)
FDA Class 2 ·Orthopedic

VOXAR VC, MODEL 1.0

FDA 510(k)
FDA Class 2 ·Radiology

PROLITE VL PULSED LIGHT SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

FDA Adverse Event
Injury ·SYNTHES USA·Product code NKB·March 25, 2015

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·April 8, 2025

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

MICRO SAGITTAL SAW

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HBE·April 26, 2011

5.0MM VARIABLE ANGLE LOCKNG SCREW/SLF-TPNG/STRDRV/40MM

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·April 29, 2013

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 11, 2014

CLICKX-3D-HEAD F/PEDICSCR POST-OPEN TAN

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013

ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

FDA Adverse Event
Injury ·SYNTHES USA·Product code NKB·December 29, 2015

CLICKX PEDICSCR Ø6.2 L50 TAN DBLUE

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013

CLICKX-3D-HEAD F/PEDICSCR POST-OPEN TAN

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013

CLICKX-3D-HEAD F/PEDICSCR POST-OPEN TAN

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013

OPTETRAK ASY,CR CEMENTED FEMORAL, SZ 2,

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 25, 2024

INSET PATELLA 26MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·October 25, 2024

ORTHOSIS,PEDICLE SPINAL FIXATION

FDA Adverse Event
Injury ·SYNTHES USA·Product code MNI·December 8, 2015