108 results
·
25ms
·
Sources: EU EUDAMED, US FDA
VENOUS M/A INTERNAL JUGULAR KIT
FDA 510(k)
FDA Class 2
·Cardiovascular
Polishers
FDA UDI
DFS - DIAMON GmbH·04057176152237·2ceram polisher cup RA
Bioseal Inc.
FDA UDI
BIOSEAL·00630094180069·Hemorrhoid Bands
ACUMED
FDA UDI
Acumed LLC·10806378043505·T15 Hexalobe Driver
Arthrex®
FDA UDI
ARTHREX, INC.·00888867042469·2 HOLE DBL COMP PLATE, 20MM
NANCY NAIL AND ENDCAP KIT
FDA UDI
Biomet Orthopedics, LLC·00887868032851·
iNSitu™ Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127026836·Shortened Dual Taper Broach, Size 20
MODIFICATION TO 3M TEGADERM CHG DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
PBN FALLOPIAN TUBE CATHETER SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE·Product code IOR·May 8, 2014
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 22, 2012
INRATIO
FDA Adverse Event
Malfunction
·BIOSITE INCORPORATED·Product code GJS·August 4, 2010
NFix II System 150 mm, Catalog number NX60150-1 spinal fusion surgery
FDA Recall
Terminated
·Synthes Spine·Product code NQP·November 7, 2008
NFix II System 200 mm, Catalog number NX60200-1. spinal fusion surgery
FDA Recall
Terminated
·Synthes Spine·Product code NQP·November 7, 2008
N-Hance System 150 mm, Catalog number NH60150-1. spinal fusion surgery
FDA Recall
Terminated
·Synthes Spine·Product code NQP·November 7, 2008
NFlex Stabilization System 150 mm, Catalog number NF60150-1. spinal fusion surgery
FDA Recall
Terminated
·Synthes Spine·Product code NPQ·November 7, 2008
NFlex Stabilization System 200 mm, Catalog number NF60020-1. spinal fusion surgery
FDA Recall
Terminated
·Synthes Spine·Product code NPQ·November 7, 2008
TI N-Hance Rod 150 mm Sterile, Catalog number 04.600.715.02S spinal fusion surgery
FDA Recall
Terminated
·Synthes Spine·Product code NQP·November 7, 2008
Synthes Bone Marrow Aspiration System, Sterile, 11 gauge, 15cm needle (without side holes) Indicated for aspirating bone marrow
FDA Recall
Terminated
·Synthes USA (HQ), Inc.·Product code FMF·January 26, 2011
Synthes Medullary Tubes
FDA Recall
Terminated
·Synthes USA (HQ), Inc.·Product code LXH·April 1, 2010