54 results · 24ms · Sources: EU EUDAMED, US FDA

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Cosmedico Ultraviolet Lamps of Various Models

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

POLYMER COATED LATEX EXAMINATION GLOVES, POWDER FREE, NON-STERILE

FDA 510(k)
FDA Class 1 ·General Hospital

MERIT BIPOLAR COAGULATION PROBE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

FDA Adverse Event
Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MAX·December 18, 2019

ZEPHYR XL DR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 13, 2014

VIRTUOSO DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 7, 2013

SAGITTAL BLADE

FDA Adverse Event
Malfunction ·STRYKER IRELAND LTD.·Product code GFA·June 22, 2011

SENRI

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·April 2, 2021

GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

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