10 results · 20ms · Sources: EU EUDAMED, US FDA

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ZIMMER M/L TAPER HIP PROSTHESIS WITH KINECTIV TECHNOLOGY SYSTEM, MODEL(S) 7848 SERIES( MODULAR NECKS), 7713 SERIES

FDA 510(k)
FDA Class 3 ·Orthopedic

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704294231·

RADIOGRAPHIC MARKERS

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

SUPERCROSS CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

MECHANICAL WALKER, ROLLATOR

FDA Adverse Event
DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code ITJ·April 22, 2013

SYNVISC

FDA Adverse Event
Injury ·Product code MOZ·April 22, 2011

LIFEPAK 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·July 8, 2008

BD ULTRA FINE¿ PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·March 11, 2020

BD ULTRA-FINE¿ MINI PEN NEEDLES 5MM (3/16¿) 31G

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·October 9, 2019

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