4,209 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NEW·April 21, 2020
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·CODMAN AND SHURTLEFF, INC·Product code NJE·September 22, 2015
UNKNOWN DCS COIL
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code HCG·September 23, 2015
UNKNOWN DCS COIL
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code HCG·September 22, 2015
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code NJE·October 29, 2015
HARMONIC ACE 5MM SHEAR
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 30, 2025
Tether Accessory For Use In The Gastrointestinal Tract
FDA classification
FDA Class 2
·Tether Accessory For Use In The Gastrointestinal Tract
WUXI FUN GLOVES CO., LTD
FDA registration
WUXI FUN GLOVES CO., LTD·3 products·🇨🇳 China
Hangzhou Dunli Medical Instruments Co.,Ltd
FDA registration
Hangzhou Dunli Medical Instruments Co.,Ltd·16 products·🇨🇳 China
YANGZHOU ZHI JUN PLASTIC PRODUCTS CO.,LTD
FDA registration
YANGZHOU ZHI JUN PLASTIC PRODUCTS CO.,LTD·1 product·🇨🇳 China
UF(II) Anatomic abutment
FDA UDI
DIO Corporation·08800049293515·
UF(II) Anatomic abutment
FDA UDI
DIO Corporation·08800049293379·
UF(II) Anatomic abutment
FDA UDI
DIO Corporation·08800049293454·
UF(II) Anatomic abutment
FDA UDI
DIO Corporation·08800049293256·
UF(II) Anatomic abutment
FDA UDI
DIO Corporation·08800049293232·
TruBase Screw
FDA UDI
Truabutment Korea Co.,Ltd·08800076409583·
TruBase
FDA UDI
Truabutment Korea Co.,Ltd·08800076406742·
TruAbutment DS
FDA UDI
TRUABUTMENT INC.·08800076446748·
UF(II) Anatomic abutment
FDA UDI
DIO Corporation·08800049293218·
TruScan Body Screw
FDA UDI
Truabutment Korea Co.,Ltd·08800076462021·