9 results
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29ms
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Sources: EU EUDAMED, US FDA
GUARDDOG OCCLUSION GUIDEWIRE, INFLATION DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
SPINE SCOPE, MODEL 2180
FDA 510(k)
FDA Class 2
·Orthopedic
SILVERSPEED HYDROPHILIC GUIDEWIRE (0.014 DIAMETER, 145CM LENGTH, SUPPORT) SILVERSPEED HYDROPHILIC GUIDEWIRE (0.014 D
FDA 510(k)
FDA Class 2
·Cardiovascular
EQUINOXE
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWT·March 26, 2019
LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X40 MM
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·April 29, 2013
SYNERGY
FDA Adverse Event
Injury
·SMITH & NEPHEW, ORTHOPEDICS·Product code JDH·May 9, 2011
ENDEAVOR ZOTAROLIMUS-ELUTING CORONARY STENT MX2
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·July 25, 2008
BIOFLO
FDA Adverse Event
Injury
·ANGIODYNAMICS, INC·Product code LJT·November 17, 2025
Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012