42 results · 23ms · Sources: EU EUDAMED, US FDA

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ReliefBand

FDA 510(k)
FDA Class 2 ·Neurology

GE XTREME INJECTOR OPTION

FDA 510(k)
FDA Class 2 ·Radiology

LABRALINK SUTURE ANCHOR WITH INSERTER, 2.9MM PER-LOADED WITH ONE (1) AND (2) #2 UHMWPE SUTURE

FDA 510(k)
FDA Class 2 ·Orthopedic

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

NIPRO BLOOD TUBING SET W/TP

FDA Adverse Event
Malfunction ·NIPRO (THAILAND) CORP. LTD.·Product code FJK·February 6, 2024

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 6, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 4, 2021

SURDIAL X

FDA Adverse Event
Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

NIPRO BLOOD TUBING SET W/TP

FDA Adverse Event
Injury ·NIPRO (THAILAND) CORP. LTD.·Product code FJK·January 17, 2024