58 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RX HERCULINK PLUS BILIARY STENT SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
COR-VALV Atrial Retractor
FDA UDI
Coroneo Inc·10817121000256·The Atrial Retractor is intended to retract atr...
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890106840·Zirlux Titanium Abutment 6 mmH compatible with:...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450216774·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033462379·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033462348·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033462386·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033462362·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033462393·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033474778·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033462355·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033486924·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033471470·
SMALL FRAGMENT DYNAMIC COMPRESSION LOCKING (DCL) SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
REAL PATIENT REAL PATIENT 128 CHANNEL EEG HEADBOX, MODEL EX-NW-128-RP
FDA 510(k)
FDA Class 2
·Neurology
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·May 28, 2025
ILET BIONIC PANCREAS
FDA Adverse Event
Malfunction
·BETA BIONICS INC.·Product code QFG·January 6, 2026
SCREW LOCKING
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES OBERDORF·Product code HWC·March 14, 2012