867 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AOS Small Bone Nailing System
FDA 510(k)
FDA Class 2
·Orthopedic
X-CORE
FDA UDI
Nuvasive, Inc.·00887517244093·X-CORE 2 Ti Endcap, Ø16x16x30mm -4°
Ceramco® II Silver™
FDA UDI
Dentsply International Inc.·D0011630140·
n/a
FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM19001632050141·Rotary instrument für surgical application
n/a
FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM19001631040141·Rotary instrument für surgical application
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613122980·Instrument Guards, Tinted Red, Vented Holes, 1/...
MIRADRY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CLAW II POLYAXIAL COMPRESSION SYSTEM AND ORTHOLOC 3DSI LOCKING SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
ZILVER 635 SELF-EXPANDING BILIARY STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·August 29, 2022
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 8, 2020
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·May 20, 2022
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·October 10, 2014
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code MMI·July 15, 2011
POLYFORM SYNTHETIC MESH
FDA Adverse Event
Injury
·PROXY BIOMEDICAL LTD.·Product code FTL·May 28, 2013
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·June 26, 2024
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·July 1, 2020
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·January 17, 2022
ZILVER 635 BILIARY SELF EXPANDING METAL STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code NIU·November 8, 2019
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 7, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 21, 2021