19 results · 24ms · Sources: EU EUDAMED, US FDA

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MODELS FAC-63 AND FAC-127 FOOT AND ANKLE COILS

FDA 510(k)
FDA Class 2 ·Radiology

PYRAMESH® Implant System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000855543·MESH 9050514 PYRM IMPL 13MMX17MMX14MM

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526827868·***DISC*LEVAMED ANKLE SUPPORT BLACK IV

PYRAMESH® Implant System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00681490484237·MESH 9050514 PYRM IMPL 13MMX17MMX14MM

ADVANCE®

FDA UDI
Microport Orthopedics Inc.·M684K00505141·

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306800887·Lister Bandage Scissors, 14cm

Nitinol Staple, Elastic Staple Small-Asymmetrical, Sterile R, Model #: a) ES-10x13x15; b) ES-10x16x19; c) ES-10x17x19; d) ES-12x13x15; e) ES-12x15x17; f) ES-12x16x19; g) ES-15x13x16

FDA Enforcement
Class II ·Terminated·TriMed Inc.·June 27, 2018

16 SOFT-X

FDA Adverse Event
Injury ·SALTER LABS·Product code CAT·August 11, 2023

PULPDENT GLAZE II

FDA 510(k)
FDA Class 2 ·Dental

RUMBAR DRAINAGE SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 8, 2013

CENTRA BED

FDA Adverse Event
Malfunction ·HILL-ROM INC.·Product code FNL·April 5, 2011

MICRONY II SR+

FDA Adverse Event
Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008

EndoVive 3s Low Profile Balloon Kits Part Number: M00548380 (XMD P/N 70-0050-514) The EndoVive 3s Low Profile Balloon is intended to provide gastric access through a gastrointestinal stoma tract for enteral feeding, medication administration and gastric decompression. The EndoVive 3s Low Profile Balloon is indicated for use in adult and pediatric patients who require long-term feeding, are unable to tolerate oral feeding, are at low risk for aspiration or require gastric decompression and/or medication delivery directly into the stomach.

FDA Enforcement
Class II ·Terminated·Xeridiem Mediem Medical Devices Inc·March 2, 2016

EndoVive 3s Low Profile Balloon Kits Part Number: M00548380 (XMD P/N 70-0050-514) The EndoVive 3s Low Profile Balloon is intended to provide gastric access through a gastrointestinal stoma tract for enteral feeding, medication administration and gastric decompression. The EndoVive 3s Low Profile Balloon is indicated for use in adult and pediatric patients who require long-term feeding, are unable to tolerate oral feeding, are at low risk for aspiration or require gastric decompression and/or medication delivery directly into the stomach.

FDA Recall
Terminated ·Xeridiem Mediem Medical Devices Inc·Product code PIF·December 23, 2015

Integra Licox Brain Tissue Oxygen Monitoring Integra Licox Recon Tissue Oxygen Monitoring 1) LICOX¿ Complete Brain Probe Kit (comprised of IP1, CC1.P1) 2) LICOX¿ Complete Brain Probe Kit (comprised of IP2, CC1.P1) 3) LICOX¿ Complete Brain Tunnelling Probe Kit (comprised of VK5.2, CC1.P1 4) LICOX¿ Complete Brain Probe Kit (comprised of IM1, CC1.SB) Sterile Rx Only Manufacturer CMS -Gesse;schaft for medizinische Sondentechnik mbH Dorfstrasse 2 24247 <eilkendorf Germany Distributed by Integra NeuroSciences 311 Enterprise Drive Plainsboro, NJ 08536, USA

FDA Enforcement
Class II ·Terminated·Integra LifeSciences Corp.·December 24, 2014

Replacement screw non-springloaded traction tongs are skull tongs for traction used to immobilize a patient with a cervical spine injury (e.g., fracture or dislocation) and sold under the CareFusion, Boss Instruments, Millennium Surgical, Prezio Health, and Stealth Surgical brand names.

FDA Enforcement
Class II ·Terminated·Instrumed International, Inc.·December 17, 2014

Gardner-Wells traction tongs are skull tongs for traction used to immobilize a patient with a cervical spine injury (e.g., fracture or dislocation) and sold under the Millenium Surgical, Echo Instruments, Adler Instrument, Surgical Direct, Stealth Surgical, CareFusion, and Boss Instruments brand names.

FDA Enforcement
Class II ·Terminated·Instrumed International, Inc.·December 17, 2014

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. Product Usage: Boston Scientific cardiac resynchronization therapy defibrillators (CRT-Ds) are indicated for patients with moderate to severe heart failure who remain symptomatic despite stable, optimal heart failure drug therapy and have left ventricular dysfunction and QRS duration > or equal to 120 ms. This family of pulse generators provide a variety of therapies including: -Ventricular tachyarrhythmia therapy, which is used to treat rhythms associated with sudden cardiac death such as VT and VF; -Cardiac Resynchronization Therapy (CRT), which treats heart failure by resynchronizing ventricular contractions through biventricular electrical stimulation; -Bradycardia pacing, including adaptive rate pacing, to detect and treat bradyarrhythmias and to provide cardiac rate support after defibrillation therapy.

FDA Enforcement
Class II ·Terminated·Boston Scientific CRM Corp·October 29, 2014