51 results · 25ms · Sources: EU EUDAMED, 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