28 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FLOWTRON UNIVERSAL, MODEL AC600
FDA 510(k)
FDA Class 2
·Cardiovascular
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964151958·Endo Carry-on Procedure Kit contains Intercept ...
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890107440·Zirlux Bite Ver Cyl Non Eng
XTRA SIGHT
FDA UDI
FGX INTERNATIONAL INC.·00193033261965·
XTRA SIGHT
FDA UDI
FGX INTERNATIONAL INC.·00193033261958·
XTRA SIGHT
FDA UDI
FGX INTERNATIONAL INC.·00193033261972·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0100440·Assembly, Caddie, Locking Caps
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0100440·Caddie, Locking Caps
OLYMPUS ENDOSCOPIC LIGATION DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MEDTRONIC AVE BRIDGE X3 STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 24, 2025
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 30, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 10, 2025
INSET I
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 25, 2025
INSET I
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·August 25, 2025
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 17, 2025
LUMAX 340 DR-T
FDA Adverse Event
Death
·BIOTRONIK SE & CO. KG·Product code MRM·March 19, 2013
DURAFORM 4X5 SPONGE SNGL
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code GXQ·March 2, 2011