98 results
·
19ms
·
Sources: EU EUDAMED, US FDA
DELTA 2000 SERIES EXTRACORPOREAL LITHOTRIPTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033505038·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033505069·
CORINNE MCCORMACK INC.
FDA UDI
FGX INTERNATIONAL INC.·00789106627556·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033505021·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033505076·
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0134110·Trial, TLIF, 27L OB STR 7Deg, 11mm
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033505045·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033505052·
AFOCUS ELECTROPYSIOLOGY CATHETER SYSTEM, MODELS 81550, 81567, 81568, 81569
FDA 510(k)
FDA Class 2
·Cardiovascular
MAGNA TEK ESU-400
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 8, 2025
QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 11, 2025
PERFECTA(R) PDA STEM COCR
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDI·December 11, 2013
2520274-2014-00674
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·February 19, 2014
2520274-2014-00670
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·February 19, 2014
2520274-2014-00676
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·February 19, 2014
UNKNOWN HIP ACETABULAR CUP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·September 4, 2019
UNKNOWN HIP FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·September 3, 2019
UNKNOWN HIP FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 4, 2019