115 results · 17ms · Sources: EU EUDAMED, US FDA

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FULL MOVEMENT THERAPY SYSTEMS

FDA 510(k)
FDA Class 2 ·Physical Medicine

3F PRO-PICC

FDA 510(k)
FDA Class 2 ·General Hospital

DRI METHADONE METABOLITE ENZYME IMMUNOASSAY

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

RADIFOCUS GLIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 22, 2018

UNICEL® DXI 600 ACCESS® IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JLW·January 22, 2013

UNKNOWN DEPUY LINER

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·December 9, 2010

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 9, 2014

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·December 29, 2025

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·May 16, 2024

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 21, 2021

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 6, 2025

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·September 15, 2023

GUIDE WIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 25, 2025

RADIFOCUS GUIDEWIRE

FDA Adverse Event
Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·December 5, 2023

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 3, 2018

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 23, 2026

RADIFOCUS GLIDEWIRE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 11, 2026

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 12, 2021

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 22, 2021

RADIFOCUS GUIDEWIRE M

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 20, 2021