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

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COLUMBIA 600 ELECTRODE, COLUMBIA 06 LEADWIRE

FDA 510(k)
FDA Class 2 ·Neurology

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014603216·Disposable Wedge Pad, Small

POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, MODEL 9043S0111

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

DUO-DENT DENTAL IMPLANT

FDA 510(k)
FDA Class 2 ·Dental

NANOKNIFE SYSTEM

FDA Adverse Event
Injury ·ANGIODYNAMICS·Product code OAB·June 9, 2015

WAVEWRITER ALPHA?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 4, 2025

ULTRACISION HARMONIC ACE (EXACT CODE UNKNOWN)

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 20, 2019

OBTRYX SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·April 26, 2013

75MM SELECTABLE NEW TLC

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 6, 2011

O2OPTIX

FDA Adverse Event
Injury ·PT CIBA VISION BATAM·Product code LPM·July 22, 2008

Malleable C- Retractor, Part Number 397.232, used to provide retraction of the soft tissues during use of trocar instrumentation. Used in the following systems: the Basic Trocar System, Universal Trocar System, Craniofacial Modular Fixation System, Craniofacial (CMF) Distraction System, MatrixORTHOGNATHIC Plating System, and the Matrix MANDIBLE Plating System.

FDA Enforcement
Class II ·Terminated·Synthes, Inc.·January 21, 2015

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

Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

FDA Enforcement
Class I ·Terminated·CareFusion 303, Inc.·August 26, 2015