9 results · 29ms · Sources: EU EUDAMED, US FDA

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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