15 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BioGuard Air/Water Valve, BioGuard Suction Valve
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CoRoent
FDA UDI
Nuvasive, Inc.·00887517637956·CoRoent Ant TLIF PEEK, 15x11x34mm 15°
OsteoMed
FDA UDI
OSTEOMED LLC·00845694046879·PrimaLIF LLIF PEEK Implant, 13mm X 18mm X 45mm,...
WEBSTER CS CATHETER WITH EZ STEER TECHNOLOGY, WEBSTER CS CATHETER WITH EZ STEER TECHNOLOGY AND AUTO ID MODEL: D-1263-04,
FDA 510(k)
FDA Class 2
·Cardiovascular
COLORED POWDER FREE AND POLYMER COATED PATIENT EXAMINATION GLOVE (PINK, BLUE, GREEN AND VIOLET)
FDA 510(k)
FDA Class 1
·General Hospital
EXPECT PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·May 19, 2026
EXPECT PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·September 24, 2025
ACQUIRE? PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·October 10, 2025
EXPECT PULMONARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·November 14, 2024
EXPECT PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FCG·April 14, 2026
*
FDA Adverse Event
Malfunction
·AVID MEDICAL, INC.·Product code KDD·May 6, 2013
TOTALCARE-
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·June 7, 2011
ERIPRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 4, 2008
EQUINOXE CAGE GLENOID S, POST AUG, RIGHT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code KWS·April 29, 2024
Medical Linear Accelerator
FDA Enforcement
Class II
·Terminated·Elekta, Inc.·September 14, 2016