484 results
·
28ms
·
Sources: EU EUDAMED, US FDA
TEH LIN POWER SCOOTER, MODEL TL-822
FDA 510(k)
FDA Class 2
·Physical Medicine
LEONE SPA
FDA UDI
LEONE SPA·08033707002130·AUSTRALIAN WIRE EXTRA SPRING HARD 12
.
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0120120·Screwdriver, NIDO Assembled Screws, Sleeved
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0120120·Screwdriver, Polyaxial, Standard
Verteview®
FDA UDI
ATLAS SPINE, INC.·M681VSS0420120·4.2mm x 12mm Self Tapping Screw
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981182571·Trial, 20x15x12mm, 7 deg. Lordosis, w/o Stops
Entuit Thrive LP
FDA UDI
XERIDIEM MEDICAL DEVICES, INC.·00827002356214·
AdaptLine
FDA UDI
Ropox A/S·05707581000737·
SYNTHETIC POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ECG HOME
FDA 510(k)
FDA Class 2
·Cardiovascular
EQUINOXE PRIMARY SHOULDER COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWS·August 25, 2022
TRANSPORT SERIES
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·December 7, 2012
PREMIUM SURGICLIP II M-11.5 TITANIUM
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY USSC PUERTO RICO·Product code FZP·April 2, 2013
PENUMBRA SYSTEM SEPARATOR 054
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code NRY·March 31, 2011
INSIGNIA AVT
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code DXY·May 8, 2008
PERMANENT PACEMAKER ELECTRODE
FDA Adverse Event
Injury
·OSCOR·Product code DTB·August 12, 2023
MAXIMO VR
FDA Adverse Event
Malfunction
·MEDTRONIC·Product code LWS·August 12, 2023
PERMANENT PACEMAKER ELECTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code DTB·August 12, 2023
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM INC.·Product code MDS·April 1, 2014
QUICKFLEX MICRO LV LEAD
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·September 9, 2013