51 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SX-One MicroKnife
FDA 510(k)
FDA Class 1
·Orthopedic
REVERSE SHOULDER PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
VASOPOUSE DEEP VEIN THROMBOSIS COMPRESSION DEVICE MODEL IPCS, MODEL SQS
FDA 510(k)
FDA Class 2
·Cardiovascular
COMPRESSION FT SCREW, 2.5 MICRO, 28MM LENGTH
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HWC·October 22, 2014
PINNACLE MTL INS NEUT36IDX60OD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·June 27, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 25, 2011
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·April 2, 2021
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 9, 2019
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 11, 2024
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 20, 2020
SENRI
FDA Adverse Event
Injury
·KANEKA·Product code LIT·March 12, 2019
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·May 6, 2025
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·December 24, 2025
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
DIVA
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 7, 2020
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020
18 SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2025
SENRI
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2025
18 SHIDEN HP
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·June 11, 2024
SENRI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 4, 2022