25 results
·
27ms
·
Sources: EU EUDAMED, US FDA
LIFESHIELD EXTENSION SET
FDA 510(k)
FDA Class 2
·General Hospital
PROFYLE
FDA UDI
Stryker GmbH·04546540211064·Combo Implant Container
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·34546540244315·BONE SCREWS, CROSS-FIT, SELF-TAPPING
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756021142·FINGER SPLINTS
McKesson
FDA UDI
MCKESSON MEDICAL-SURGICAL INC.·20612479259496·Medical Face Masks EAR-LOOP / PLEATED STYLE | ...
Novo Surgical
FDA UDI
NOVO SURGICAL, INC.·G5869121030·flat caps, gas or steam permeable, can be used ...
Malibu
FDA UDI
Seaspine Orthopedics Corporation·10889981080501·Bone Probe, Curved
Arthrex®
FDA UDI
ARTHREX, INC.·00888867057432·UNIVERSAL GLENOID - INLAY LARGE
BANDVIEW SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
UNIVERSAL GLENOID - INLAY LARGE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code PHX·June 21, 2024
UNIVERSAL GLENOID - INLAY LARGE
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·April 30, 2019
UNIVERSAL GLENOID - INLAY LARGE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code PHX·December 28, 2020
LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·January 11, 2013
FREESTYLE FREEDOM
FDA Adverse Event
Injury
·Product code NBW·December 1, 2010
PLEURX PLEURAL CATHETER MINI KIT
FDA Adverse Event
Malfunction
·CAREFUSION·Product code DWM·July 3, 2014
UNIVERSAL GLENOID - INLAY LARGE
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code PHX·June 20, 2024
UNIVERSAL GLENOID - INLAY LARGE PLUS
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code PHX·June 20, 2024
UNI GLENOID-PERIPHERAL LOCK SCRW
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·July 26, 2024
ECLIPSE TRUNION,45 MM TPS CTD
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·July 26, 2024