26 results
·
25ms
·
Sources: EU EUDAMED, US FDA
BD Univia RightFit Enteral Extension Sets and Transitional Adapters
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252133728·ACTIVATION ROD FLEXIBLE
OsteoMed
FDA UDI
OSTEOMED LLC·00845694006040·M3 Drill and Driver Organizer
OsteoMed
FDA UDI
OSTEOMED LLC·00845694010948·M3-X Drill and Driver Organizer
ERECAID CLASSIC SYSTEM; ERECAID ESTEEM MANUAL SYSTEM; ERECAID ESTEEM BATTERY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Anterior Spine Truss System Stand Alone (ASTS-SA) Interbody Fusion Device
FDA 510(k)
FDA Class 2
·Orthopedic
PRECISION SPECTRA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 6, 2024
BIOSTEON INTRALINE
FDA Adverse Event
Malfunction
·BIOCOMPOSITES LTD.·Product code LOE·September 22, 2020
MICROSTAAR INJECTOR
FDA Adverse Event
Malfunction
·STAAR SURGICAL CO.·Product code KYB·October 15, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011
EXPEDIUM 5.5 SS 30MM ROD
FDA Adverse Event
Injury
·DEPUY SYNTHES SPINE·Product code KWP·July 1, 2013
NIBP CUFFS
FDA Adverse Event
Malfunction
·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code OED·March 5, 2026
NIBP CUFFS
FDA Adverse Event
Malfunction
·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code OED·January 7, 2026
7.5MM REVERE PEDICLE SCREW 45MM
FDA Adverse Event
Other
·GLOBUS MEDICAL, INC.·Product code MCV·July 11, 2007
6.5MM REVERE PEDICLE SCREW 35MM
FDA Adverse Event
Other
·GLOBUS MEDICAL, INC.·Product code MCV·July 25, 2007
6.5MM REVERE PEDICLE SCREW 40MM
FDA Adverse Event
Other
·GLOBUS MEDICAL, INC.·Product code MCV·April 7, 2008
7.5MM REVERE PEDICLE SCREW 40MM
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code MCV·June 18, 2008
6.5MM REVERE PEDICLE SCREW 40MM
FDA Adverse Event
Injury
·GLOBUS MEDICAL, INC.·Product code MCV·June 6, 2008
7.5MM REVERE PEDICLE SCREW 40MM
FDA Adverse Event
Other
·GLOBUS MEDICAL, INC.·Product code MCV·January 31, 2008
UNKNOWN GII ANCHOR
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code JDR·October 28, 2019