66 results · 30ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

MOUTHGUARD AND ALIGNER MATERIALS

FDA 510(k)
FDA Unclassified ·Unknown

PORTA SMK 82, MODEL 2032

FDA 510(k)
FDA Class 2 ·Dental

XPS NITRO SYSTEM

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

ALIGN TO URETHRAL SUPPORT SYSTEM

FDA Adverse Event
Injury ·C.R. BARD, INC. (COVINGTON)·Product code FTL·April 12, 2013

ARCHITECT IVANCOMYCIN

FDA Adverse Event
Malfunction ·ABBOTT GERMANY·Product code LEH·April 19, 2011

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 18, 2008

GLIDESHEATH

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·August 7, 2019

UNSPECIFIED SAFESET TRANSPAC SETS

FDA Adverse Event
Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

GLIDESHEATH

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·July 7, 2022

GLIDESHEATH

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·December 1, 2020

RADIFOCUS INTRODUCER

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·May 19, 2022

RADIFOCUS INTRODUCER

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·January 21, 2022

RADIFOCUS INTRODUCER

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·June 25, 2020

RADIFOCUS INTRODUCER

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·June 25, 2020

RADIFOCUS INTRODUCER

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·June 29, 2020

RADIFOCUS INTRODUCER

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·December 2, 2021

RADIFOCUS INTRODUCER

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·May 18, 2022

GLIDESHEATH

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·October 9, 2018

GLIDESHEATH

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·November 3, 2020

GLIDESHEATH

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·October 30, 2020