11 results
·
18ms
·
Sources: EU EUDAMED, US FDA
WIZARD PEDIATRIC WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704262414·
Valencia Pedicle Screw System
FDA UDI
Altus Spine, LLC·B41799345601·4.5mm x 60mm Triple Lead Closed Head Screw
VALLEYLAB LAPAROSCOPIC HANDSWITCH/ELECTRODES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
VITEX P.D.A
FDA 510(k)
FDA Class 2
·Dental
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 10, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 4, 2014
EON RECHARGEABLE IPG
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·November 23, 2010
TMJ SYSTEM LEFT STANDARD MANDIBULAR COMPONENT 55MM / 12 HOLE
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code LZD·December 4, 2020
TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code LZD·December 4, 2020
UNKNOWN RIGHT FOSSA
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code LZD·December 4, 2020