28 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TempSure
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293227·
Sklar®
FDA UDI
SKLAR CORPORATION·10649111140532·RANKIN KELLY FCP STR 6.25"
FLEXI-LITE
FDA 510(k)
FDA Class 2
·Anesthesiology
ELECTROSURGICAL MONOPOLAR CABLE/ADAPTERS, ELECTROSURGICAL BIPOLAR CABLE/ ADAPTERS, BIPOLAR ELECTROSURGICAL CABLES, MONOP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·April 4, 2022
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·February 22, 2022
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·February 2, 2022
VITALITY 2
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 21, 2011
PENUMBRA RUBY COIL
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code KRD·June 14, 2013
UNKNOWN DEPUY PINNACLE METAL HEAD 36MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWY·September 19, 2008
Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
FDA Enforcement
Class II
·Terminated·Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical·June 12, 2019
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·November 23, 2022
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·Product code ITX·May 25, 2021
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·April 16, 2024
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Injury
·COOK VANDERGRIFT INC·Product code ITX·April 2, 2024
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Malfunction
·COOK VASCULAR INC·Product code ITX·September 5, 2018
COOK-SWARTZ DOPPLER PROBE
FDA Adverse Event
Malfunction
·COOK VANDERGRIFT INC·Product code ITX·October 31, 2023
OPEN-END FLEXI-TIP URETERAL CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KOD·February 6, 2020
OPEN-END URETERAL CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KOD·February 7, 2020