34 results · 27ms · Sources: EU EUDAMED, US FDA

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HeatLux Pro II

FDA 510(k)
FDA Class 2 ·Physical Medicine

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704283549·LAHEY FINGER RETRACTOR 4 3/4" 3 PRONG SHARP

BREATHING FILTER BACTERIAL/VIRAL, MODEL AG7178

FDA 510(k)
FDA Class 2 ·Anesthesiology

TYVEK SELF-SEAL POUCHES ,TYVEK HEAT-SEAL ROLLS

FDA 510(k)
FDA Class 2 ·General Hospital

PELVICOL ACEELUAR COLLAGEN MATRIX

FDA Adverse Event
Injury ·TISSUE SCIENCE LABORATORIES·Product code FTL·May 29, 2013

COLLEAGUE PRE 1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011

TRANSDUCER LINE SET-TRIPLE SET

FDA Adverse Event
Other ·EDWARDS LIFESCIENCES CORP.·Product code DRS·September 4, 2008

SHIDEN HP

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·June 4, 2019

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

KYPHON BONE CEMENT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·April 23, 2019

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

METACROSS OTW PTA BALLOON DILATATION CATHETER

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2019

1030489-2019-01423

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NDN·December 13, 2019

SHIDEN HP

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·March 1, 2024

OHICHO NEO

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·February 7, 2024

SHIDEN

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 10, 2020

OHICHO3

FDA Adverse Event
Injury ·Product code LIT·December 26, 2019

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