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

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CAPROSYN ABSORBABLE SUTURE

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

Baltic Denture System BD Load

FDA UDI
Merz Dental GmbH·D7091032586·Baltic Denture System BDLoad Lw6 PLSEbil2DFl D2...

ANTERIOR STABILIZED TIBIAL BEARINGS

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDPOR PTERIONAL SURGICAL IMPLANT

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

SMALL PERIPHERAL CUTTING BALLOON®

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LIT·April 3, 2013

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·March 29, 2011

PULSE GEN MODEL 100

FDA Adverse Event
Malfunction ·CYBERONICS, INC.·Product code LYJ·April 21, 2008

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

The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018

Boston Scientific COGNIS CRT-D, Cardiac Resynchronization Therapy Defibrillator, models N118, N119. The following models are not available in the US: models N106, N107, P106, P107. Sterilized using ethylene oxide. Boston Scientific, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA. Indicated for patients who are at risk for sudden cardiac death due to ventricular arrhythmias and may require pacing support.

FDA Enforcement
Class II ·Terminated·Boston Scientific CRM Corp·October 23, 2013

OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

FDA Enforcement
Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012