12 results · 22ms · Sources: EU EUDAMED, US FDA

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AVANDX E. FAECALIS/OE PNA FISH CULTURE IDENTIFICATION KIT

FDA 510(k)
FDA Class 1 ·Microbiology

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·January 10, 2018

IMBIBE BONE MARROW ASPIRATION SYRINGE

FDA 510(k)
FDA Class 2 ·General Hospital

INION GTR BIODEGRADABLE MEMBRANE SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 22, 2019

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 14, 2018

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 5, 2018

1/8" HEX DRIVE

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·April 29, 2013

ON-Q C-BLOC SAF/PCA

FDA Adverse Event
Malfunction ·I-FLOW CORP.·Product code MEB·March 31, 2011

HIRES 90K

FDA Adverse Event
Malfunction ·ADVANCED BIONICS, LLC·Product code MCM·March 12, 2008

On-Board Imager - Exact Arm Elbow Motor Shaft (kVD, kVS, and MV) with ''Type 01" elbow motors. Product Usage: The On-Board Imager device is an x-ray device used for evaluation of correct patient position in relation to isocenter and verification of treatment fields in relation to anatomical and fiducial landmarks.

FDA Enforcement
Class II ·Terminated·Varian Medical Systems, Inc.·April 30, 2014

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