26 results
·
25ms
·
Sources: EU EUDAMED, US FDA
EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Axcent Acrylics
FDA UDI
GARRECO, LLC·D79330104250·Repair Lt Char 25lb
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890104250·Zirlux 30 Degree Multi-Unit Abutment 4 mmH comp...
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0100250·Caddie Lid, Fixed Cross Links 5.5mm
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0100250·Caddie Lid, Fixed Cross Links, 5.5mm
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL UM-D·Product code FPA·January 27, 2026
ELECTRICATOR MODEL 26000
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ISOBAR SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·November 18, 2025
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 11, 2007
THERMOCOOL® SF NAV BI-DIRECTIONAL CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code LPB·March 19, 2013
HYPODERMIC NEEDLE
FDA Adverse Event
Injury
·Product code FMI·March 4, 2011
CELSITE ACCESS PORT
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL SAS·Product code LJT·October 23, 2014
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·December 22, 2011
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011
UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011